Homozygous prion protein genotype predisposes to sporadic Creutzfeldt–Jakob disease
[Auszug] The prion protein (PrP) gene encodes a normal cell-surface glycoprotein found on neuronal cells, lymphocytes and other tissues7'8. Coding mutations (Fig. 1) have been found in familial CJD, GSS and also in atypical familial dementias now known to be part ...
Autor*in: |
Palmer, Mark S. [verfasserIn] Dryden, Aidan J. [verfasserIn] Hughes, J. Trevor [verfasserIn] |
---|
Format: |
E-Artikel |
---|---|
Sprache: |
Englisch |
Erschienen: |
s.l.: Nature Publishing Group ; 1991 |
---|
Umfang: |
3 |
---|
Reproduktion: |
Nature Archives 1869 - 2009 |
---|---|
Übergeordnetes Werk: |
In: Nature |
Übergeordnetes Werk: |
volume:352 ; year:1991 ; number:6333 ; month:02 ; pages:340-342 ; extent:3 |
Links: |
---|
DOI / URN: |
10.1038/352340a0 |
---|
Katalog-ID: |
NLEJ235191213 |
---|
LEADER | 01000caa a22002652 4500 | ||
---|---|---|---|
001 | NLEJ235191213 | ||
003 | DE-627 | ||
005 | 20230506100344.0 | ||
007 | cr uuu---uuuuu | ||
008 | 110225s1991 xx |||||o 00| ||eng c | ||
024 | 7 | |a 10.1038/352340a0 |2 doi | |
035 | |a (DE-627)NLEJ235191213 | ||
040 | |a DE-627 |b ger |c DE-627 |e rakwb | ||
041 | |a eng | ||
100 | 1 | |a Palmer, Mark S. |e verfasserin |4 aut | |
245 | 1 | 0 | |a Homozygous prion protein genotype predisposes to sporadic Creutzfeldt–Jakob disease |
264 | 1 | |a [s.l.] |b Nature Publishing Group |c 1991 | |
300 | |a 3 | ||
336 | |a nicht spezifiziert |b zzz |2 rdacontent | ||
337 | |a nicht spezifiziert |b z |2 rdamedia | ||
338 | |a nicht spezifiziert |b zu |2 rdacarrier | ||
520 | |a [Auszug] The prion protein (PrP) gene encodes a normal cell-surface glycoprotein found on neuronal cells, lymphocytes and other tissues7'8. Coding mutations (Fig. 1) have been found in familial CJD, GSS and also in atypical familial dementias now known to be part ... | ||
533 | |f Nature Archives 1869 - 2009 | ||
700 | 1 | |a Dryden, Aidan J. |e verfasserin |4 aut | |
700 | 1 | |a Hughes, J. Trevor |e verfasserin |4 aut | |
700 | 1 | |a Collinge, John |4 oth | |
773 | 0 | 8 | |i In |t Nature <London> |d London [u.a.] : Nature Publising Group, 1869 |g 352(1991), 6333 vom: Feb., Seite 340-342 |w (DE-627)NLEJ227682335 |w (DE-600)1413423-8 |x 1476-4687 |7 nnns |
773 | 1 | 8 | |g volume:352 |g year:1991 |g number:6333 |g month:02 |g pages:340-342 |g extent:3 |
856 | 4 | 0 | |u http://dx.doi.org/10.1038/352340a0 |q application/pdf |z Deutschlandweit zugänglich |
912 | |a GBV_USEFLAG_U | ||
912 | |a ZDB-1-NTA | ||
912 | |a GBV_NL_ARTICLE | ||
951 | |a AR | ||
952 | |d 352 |j 1991 |e 6333 |c 2 |h 340-342 |g 3 |
author_variant |
m s p ms msp a j d aj ajd j t h jt jth |
---|---|
matchkey_str |
article:14764687:1991----::ooyosropoeneoyerdsoetsoaice |
hierarchy_sort_str |
1991 |
publishDate |
1991 |
allfields |
10.1038/352340a0 doi (DE-627)NLEJ235191213 DE-627 ger DE-627 rakwb eng Palmer, Mark S. verfasserin aut Homozygous prion protein genotype predisposes to sporadic Creutzfeldt–Jakob disease [s.l.] Nature Publishing Group 1991 3 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier [Auszug] The prion protein (PrP) gene encodes a normal cell-surface glycoprotein found on neuronal cells, lymphocytes and other tissues7'8. Coding mutations (Fig. 1) have been found in familial CJD, GSS and also in atypical familial dementias now known to be part ... Nature Archives 1869 - 2009 Dryden, Aidan J. verfasserin aut Hughes, J. Trevor verfasserin aut Collinge, John oth In Nature <London> London [u.a.] : Nature Publising Group, 1869 352(1991), 6333 vom: Feb., Seite 340-342 (DE-627)NLEJ227682335 (DE-600)1413423-8 1476-4687 nnns volume:352 year:1991 number:6333 month:02 pages:340-342 extent:3 http://dx.doi.org/10.1038/352340a0 application/pdf Deutschlandweit zugänglich GBV_USEFLAG_U ZDB-1-NTA GBV_NL_ARTICLE AR 352 1991 6333 2 340-342 3 |
spelling |
10.1038/352340a0 doi (DE-627)NLEJ235191213 DE-627 ger DE-627 rakwb eng Palmer, Mark S. verfasserin aut Homozygous prion protein genotype predisposes to sporadic Creutzfeldt–Jakob disease [s.l.] Nature Publishing Group 1991 3 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier [Auszug] The prion protein (PrP) gene encodes a normal cell-surface glycoprotein found on neuronal cells, lymphocytes and other tissues7'8. Coding mutations (Fig. 1) have been found in familial CJD, GSS and also in atypical familial dementias now known to be part ... Nature Archives 1869 - 2009 Dryden, Aidan J. verfasserin aut Hughes, J. Trevor verfasserin aut Collinge, John oth In Nature <London> London [u.a.] : Nature Publising Group, 1869 352(1991), 6333 vom: Feb., Seite 340-342 (DE-627)NLEJ227682335 (DE-600)1413423-8 1476-4687 nnns volume:352 year:1991 number:6333 month:02 pages:340-342 extent:3 http://dx.doi.org/10.1038/352340a0 application/pdf Deutschlandweit zugänglich GBV_USEFLAG_U ZDB-1-NTA GBV_NL_ARTICLE AR 352 1991 6333 2 340-342 3 |
allfields_unstemmed |
10.1038/352340a0 doi (DE-627)NLEJ235191213 DE-627 ger DE-627 rakwb eng Palmer, Mark S. verfasserin aut Homozygous prion protein genotype predisposes to sporadic Creutzfeldt–Jakob disease [s.l.] Nature Publishing Group 1991 3 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier [Auszug] The prion protein (PrP) gene encodes a normal cell-surface glycoprotein found on neuronal cells, lymphocytes and other tissues7'8. Coding mutations (Fig. 1) have been found in familial CJD, GSS and also in atypical familial dementias now known to be part ... Nature Archives 1869 - 2009 Dryden, Aidan J. verfasserin aut Hughes, J. Trevor verfasserin aut Collinge, John oth In Nature <London> London [u.a.] : Nature Publising Group, 1869 352(1991), 6333 vom: Feb., Seite 340-342 (DE-627)NLEJ227682335 (DE-600)1413423-8 1476-4687 nnns volume:352 year:1991 number:6333 month:02 pages:340-342 extent:3 http://dx.doi.org/10.1038/352340a0 application/pdf Deutschlandweit zugänglich GBV_USEFLAG_U ZDB-1-NTA GBV_NL_ARTICLE AR 352 1991 6333 2 340-342 3 |
allfieldsGer |
10.1038/352340a0 doi (DE-627)NLEJ235191213 DE-627 ger DE-627 rakwb eng Palmer, Mark S. verfasserin aut Homozygous prion protein genotype predisposes to sporadic Creutzfeldt–Jakob disease [s.l.] Nature Publishing Group 1991 3 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier [Auszug] The prion protein (PrP) gene encodes a normal cell-surface glycoprotein found on neuronal cells, lymphocytes and other tissues7'8. Coding mutations (Fig. 1) have been found in familial CJD, GSS and also in atypical familial dementias now known to be part ... Nature Archives 1869 - 2009 Dryden, Aidan J. verfasserin aut Hughes, J. Trevor verfasserin aut Collinge, John oth In Nature <London> London [u.a.] : Nature Publising Group, 1869 352(1991), 6333 vom: Feb., Seite 340-342 (DE-627)NLEJ227682335 (DE-600)1413423-8 1476-4687 nnns volume:352 year:1991 number:6333 month:02 pages:340-342 extent:3 http://dx.doi.org/10.1038/352340a0 application/pdf Deutschlandweit zugänglich GBV_USEFLAG_U ZDB-1-NTA GBV_NL_ARTICLE AR 352 1991 6333 2 340-342 3 |
allfieldsSound |
10.1038/352340a0 doi (DE-627)NLEJ235191213 DE-627 ger DE-627 rakwb eng Palmer, Mark S. verfasserin aut Homozygous prion protein genotype predisposes to sporadic Creutzfeldt–Jakob disease [s.l.] Nature Publishing Group 1991 3 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier [Auszug] The prion protein (PrP) gene encodes a normal cell-surface glycoprotein found on neuronal cells, lymphocytes and other tissues7'8. Coding mutations (Fig. 1) have been found in familial CJD, GSS and also in atypical familial dementias now known to be part ... Nature Archives 1869 - 2009 Dryden, Aidan J. verfasserin aut Hughes, J. Trevor verfasserin aut Collinge, John oth In Nature <London> London [u.a.] : Nature Publising Group, 1869 352(1991), 6333 vom: Feb., Seite 340-342 (DE-627)NLEJ227682335 (DE-600)1413423-8 1476-4687 nnns volume:352 year:1991 number:6333 month:02 pages:340-342 extent:3 http://dx.doi.org/10.1038/352340a0 application/pdf Deutschlandweit zugänglich GBV_USEFLAG_U ZDB-1-NTA GBV_NL_ARTICLE AR 352 1991 6333 2 340-342 3 |
language |
English |
source |
In Nature <London> 352(1991), 6333 vom: Feb., Seite 340-342 volume:352 year:1991 number:6333 month:02 pages:340-342 extent:3 |
sourceStr |
In Nature <London> 352(1991), 6333 vom: Feb., Seite 340-342 volume:352 year:1991 number:6333 month:02 pages:340-342 extent:3 |
format_phy_str_mv |
Article |
institution |
findex.gbv.de |
isfreeaccess_bool |
false |
container_title |
Nature <London> |
authorswithroles_txt_mv |
Palmer, Mark S. @@aut@@ Dryden, Aidan J. @@aut@@ Hughes, J. Trevor @@aut@@ Collinge, John @@oth@@ |
publishDateDaySort_date |
1991-02-01T00:00:00Z |
hierarchy_top_id |
NLEJ227682335 |
id |
NLEJ235191213 |
language_de |
englisch |
fullrecord |
<?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>01000caa a22002652 4500</leader><controlfield tag="001">NLEJ235191213</controlfield><controlfield tag="003">DE-627</controlfield><controlfield tag="005">20230506100344.0</controlfield><controlfield tag="007">cr uuu---uuuuu</controlfield><controlfield tag="008">110225s1991 xx |||||o 00| ||eng c</controlfield><datafield tag="024" ind1="7" ind2=" "><subfield code="a">10.1038/352340a0</subfield><subfield code="2">doi</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-627)NLEJ235191213</subfield></datafield><datafield tag="040" ind1=" " ind2=" "><subfield code="a">DE-627</subfield><subfield code="b">ger</subfield><subfield code="c">DE-627</subfield><subfield code="e">rakwb</subfield></datafield><datafield tag="041" ind1=" " ind2=" "><subfield code="a">eng</subfield></datafield><datafield tag="100" ind1="1" ind2=" "><subfield code="a">Palmer, Mark S.</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Homozygous prion protein genotype predisposes to sporadic Creutzfeldt–Jakob disease</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="a">[s.l.]</subfield><subfield code="b">Nature Publishing Group</subfield><subfield code="c">1991</subfield></datafield><datafield tag="300" ind1=" " ind2=" "><subfield code="a">3</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="a">nicht spezifiziert</subfield><subfield code="b">zzz</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="a">nicht spezifiziert</subfield><subfield code="b">z</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="a">nicht spezifiziert</subfield><subfield code="b">zu</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">[Auszug] The prion protein (PrP) gene encodes a normal cell-surface glycoprotein found on neuronal cells, lymphocytes and other tissues7'8. Coding mutations (Fig. 1) have been found in familial CJD, GSS and also in atypical familial dementias now known to be part ...</subfield></datafield><datafield tag="533" ind1=" " ind2=" "><subfield code="f">Nature Archives 1869 - 2009</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Dryden, Aidan J.</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Hughes, J. Trevor</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Collinge, John</subfield><subfield code="4">oth</subfield></datafield><datafield tag="773" ind1="0" ind2="8"><subfield code="i">In</subfield><subfield code="t">Nature <London></subfield><subfield code="d">London [u.a.] : Nature Publising Group, 1869</subfield><subfield code="g">352(1991), 6333 vom: Feb., Seite 340-342</subfield><subfield code="w">(DE-627)NLEJ227682335</subfield><subfield code="w">(DE-600)1413423-8</subfield><subfield code="x">1476-4687</subfield><subfield code="7">nnns</subfield></datafield><datafield tag="773" ind1="1" ind2="8"><subfield code="g">volume:352</subfield><subfield code="g">year:1991</subfield><subfield code="g">number:6333</subfield><subfield code="g">month:02</subfield><subfield code="g">pages:340-342</subfield><subfield code="g">extent:3</subfield></datafield><datafield tag="856" ind1="4" ind2="0"><subfield code="u">http://dx.doi.org/10.1038/352340a0</subfield><subfield code="q">application/pdf</subfield><subfield code="z">Deutschlandweit zugänglich</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_USEFLAG_U</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">ZDB-1-NTA</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_NL_ARTICLE</subfield></datafield><datafield tag="951" ind1=" " ind2=" "><subfield code="a">AR</subfield></datafield><datafield tag="952" ind1=" " ind2=" "><subfield code="d">352</subfield><subfield code="j">1991</subfield><subfield code="e">6333</subfield><subfield code="c">2</subfield><subfield code="h">340-342</subfield><subfield code="g">3</subfield></datafield></record></collection>
|
series2 |
Nature Archives 1869 - 2009 |
author |
Palmer, Mark S. |
spellingShingle |
Palmer, Mark S. Homozygous prion protein genotype predisposes to sporadic Creutzfeldt–Jakob disease |
authorStr |
Palmer, Mark S. |
ppnlink_with_tag_str_mv |
@@773@@(DE-627)NLEJ227682335 |
format |
electronic Article |
delete_txt_mv |
keep |
author_role |
aut aut aut |
collection |
NL |
publishPlace |
[s.l.] |
remote_str |
true |
illustrated |
Not Illustrated |
issn |
1476-4687 |
topic_title |
Homozygous prion protein genotype predisposes to sporadic Creutzfeldt–Jakob disease |
publisher |
Nature Publishing Group |
publisherStr |
Nature Publishing Group |
format_facet |
Elektronische Aufsätze Aufsätze Elektronische Ressource |
format_main_str_mv |
Text Zeitschrift/Artikel |
carriertype_str_mv |
zu |
author2_variant |
j c jc |
hierarchy_parent_title |
Nature <London> |
hierarchy_parent_id |
NLEJ227682335 |
hierarchy_top_title |
Nature <London> |
isfreeaccess_txt |
false |
familylinks_str_mv |
(DE-627)NLEJ227682335 (DE-600)1413423-8 |
title |
Homozygous prion protein genotype predisposes to sporadic Creutzfeldt–Jakob disease |
ctrlnum |
(DE-627)NLEJ235191213 |
title_full |
Homozygous prion protein genotype predisposes to sporadic Creutzfeldt–Jakob disease |
author_sort |
Palmer, Mark S. |
journal |
Nature <London> |
journalStr |
Nature <London> |
lang_code |
eng |
isOA_bool |
false |
recordtype |
marc |
publishDateSort |
1991 |
contenttype_str_mv |
zzz |
container_start_page |
340 |
author_browse |
Palmer, Mark S. Dryden, Aidan J. Hughes, J. Trevor |
container_volume |
352 |
physical |
3 |
format_se |
Elektronische Aufsätze |
author-letter |
Palmer, Mark S. |
doi_str_mv |
10.1038/352340a0 |
author2-role |
verfasserin |
title_sort |
homozygous prion protein genotype predisposes to sporadic creutzfeldt–jakob disease |
title_auth |
Homozygous prion protein genotype predisposes to sporadic Creutzfeldt–Jakob disease |
abstract |
[Auszug] The prion protein (PrP) gene encodes a normal cell-surface glycoprotein found on neuronal cells, lymphocytes and other tissues7'8. Coding mutations (Fig. 1) have been found in familial CJD, GSS and also in atypical familial dementias now known to be part ... |
abstractGer |
[Auszug] The prion protein (PrP) gene encodes a normal cell-surface glycoprotein found on neuronal cells, lymphocytes and other tissues7'8. Coding mutations (Fig. 1) have been found in familial CJD, GSS and also in atypical familial dementias now known to be part ... |
abstract_unstemmed |
[Auszug] The prion protein (PrP) gene encodes a normal cell-surface glycoprotein found on neuronal cells, lymphocytes and other tissues7'8. Coding mutations (Fig. 1) have been found in familial CJD, GSS and also in atypical familial dementias now known to be part ... |
collection_details |
GBV_USEFLAG_U ZDB-1-NTA GBV_NL_ARTICLE |
container_issue |
6333 |
title_short |
Homozygous prion protein genotype predisposes to sporadic Creutzfeldt–Jakob disease |
url |
http://dx.doi.org/10.1038/352340a0 |
remote_bool |
true |
author2 |
Dryden, Aidan J. Hughes, J. Trevor Collinge, John |
author2Str |
Dryden, Aidan J. Hughes, J. Trevor Collinge, John |
ppnlink |
NLEJ227682335 |
mediatype_str_mv |
z |
isOA_txt |
false |
hochschulschrift_bool |
false |
author2_role |
oth |
doi_str |
10.1038/352340a0 |
up_date |
2024-07-06T07:41:54.100Z |
_version_ |
1803814661364121600 |
fullrecord_marcxml |
<?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>01000caa a22002652 4500</leader><controlfield tag="001">NLEJ235191213</controlfield><controlfield tag="003">DE-627</controlfield><controlfield tag="005">20230506100344.0</controlfield><controlfield tag="007">cr uuu---uuuuu</controlfield><controlfield tag="008">110225s1991 xx |||||o 00| ||eng c</controlfield><datafield tag="024" ind1="7" ind2=" "><subfield code="a">10.1038/352340a0</subfield><subfield code="2">doi</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-627)NLEJ235191213</subfield></datafield><datafield tag="040" ind1=" " ind2=" "><subfield code="a">DE-627</subfield><subfield code="b">ger</subfield><subfield code="c">DE-627</subfield><subfield code="e">rakwb</subfield></datafield><datafield tag="041" ind1=" " ind2=" "><subfield code="a">eng</subfield></datafield><datafield tag="100" ind1="1" ind2=" "><subfield code="a">Palmer, Mark S.</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Homozygous prion protein genotype predisposes to sporadic Creutzfeldt–Jakob disease</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="a">[s.l.]</subfield><subfield code="b">Nature Publishing Group</subfield><subfield code="c">1991</subfield></datafield><datafield tag="300" ind1=" " ind2=" "><subfield code="a">3</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="a">nicht spezifiziert</subfield><subfield code="b">zzz</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="a">nicht spezifiziert</subfield><subfield code="b">z</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="a">nicht spezifiziert</subfield><subfield code="b">zu</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">[Auszug] The prion protein (PrP) gene encodes a normal cell-surface glycoprotein found on neuronal cells, lymphocytes and other tissues7'8. Coding mutations (Fig. 1) have been found in familial CJD, GSS and also in atypical familial dementias now known to be part ...</subfield></datafield><datafield tag="533" ind1=" " ind2=" "><subfield code="f">Nature Archives 1869 - 2009</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Dryden, Aidan J.</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Hughes, J. Trevor</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Collinge, John</subfield><subfield code="4">oth</subfield></datafield><datafield tag="773" ind1="0" ind2="8"><subfield code="i">In</subfield><subfield code="t">Nature <London></subfield><subfield code="d">London [u.a.] : Nature Publising Group, 1869</subfield><subfield code="g">352(1991), 6333 vom: Feb., Seite 340-342</subfield><subfield code="w">(DE-627)NLEJ227682335</subfield><subfield code="w">(DE-600)1413423-8</subfield><subfield code="x">1476-4687</subfield><subfield code="7">nnns</subfield></datafield><datafield tag="773" ind1="1" ind2="8"><subfield code="g">volume:352</subfield><subfield code="g">year:1991</subfield><subfield code="g">number:6333</subfield><subfield code="g">month:02</subfield><subfield code="g">pages:340-342</subfield><subfield code="g">extent:3</subfield></datafield><datafield tag="856" ind1="4" ind2="0"><subfield code="u">http://dx.doi.org/10.1038/352340a0</subfield><subfield code="q">application/pdf</subfield><subfield code="z">Deutschlandweit zugänglich</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_USEFLAG_U</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">ZDB-1-NTA</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_NL_ARTICLE</subfield></datafield><datafield tag="951" ind1=" " ind2=" "><subfield code="a">AR</subfield></datafield><datafield tag="952" ind1=" " ind2=" "><subfield code="d">352</subfield><subfield code="j">1991</subfield><subfield code="e">6333</subfield><subfield code="c">2</subfield><subfield code="h">340-342</subfield><subfield code="g">3</subfield></datafield></record></collection>
|
score |
7.4012003 |