Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21

Gespeichert in:

Autor*in:	Cruts, Marc [verfasserIn] Gijselinck, Ilse van der Zee, Julie Engelborghs, Sebastiaan Wils, Hans Pirici, Daniel Rademakers, Rosa Vandenberghe, Rik Dermaut, Bart Martin, Jean-Jacques van Duijn, Cornelia Peeters, Karin Sciot, Raf Santens, Patrick De Pooter, Tim Mattheijssens, Maria Van den Broeck, Marleen Cuijt, Ivy Vennekens, Krist'l

Format:	Artikel

Erschienen:	2006

Umfang:	5

Übergeordnetes Werk:	Enthalten in: Nature - London : Macmillan Publishers Limited, part of Springer Nature, 1869, 442(2006), 7105, Seite 920-924
Übergeordnetes Werk:	volume:442 ; year:2006 ; number:7105 ; pages:920-924 ; extent:5

Katalog-ID:	OLC1723616915

Internformat


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allfields	sw060825 (DE-627)OLC1723616915 (DE-599)GBVOLC1723616915 DE-627 ger DE-627 rakwb 070 500 500 AVZ BIODIV fid Cruts, Marc verfasserin aut Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21 2006 5 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier Gijselinck, Ilse oth van der Zee, Julie oth Engelborghs, Sebastiaan oth Wils, Hans oth Pirici, Daniel oth Rademakers, Rosa oth Vandenberghe, Rik oth Dermaut, Bart oth Martin, Jean-Jacques oth van Duijn, Cornelia oth Peeters, Karin oth Sciot, Raf oth Santens, Patrick oth De Pooter, Tim oth Mattheijssens, Maria oth Van den Broeck, Marleen oth Cuijt, Ivy oth Vennekens, Krist'l oth Enthalten in Nature London : Macmillan Publishers Limited, part of Springer Nature, 1869 442(2006), 7105, Seite 920-924 (DE-627)129292834 (DE-600)120714-3 (DE-576)014473941 0028-0836 nnns volume:442 year:2006 number:7105 pages:920-924 extent:5 GBV_USEFLAG_A SYSFLAG_A GBV_OLC FID-BIODIV SSG-OLC-PHY SSG-OLC-CHE SSG-OLC-MAT SSG-OLC-FOR SSG-OLC-SPO SSG-OLC-PHA SSG-OLC-DE-84 SSG-OPC-FOR GBV_ILN_11 GBV_ILN_20 GBV_ILN_21 GBV_ILN_22 GBV_ILN_23 GBV_ILN_30 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_47 GBV_ILN_55 GBV_ILN_59 GBV_ILN_60 GBV_ILN_62 GBV_ILN_69 GBV_ILN_70 GBV_ILN_95 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_130 GBV_ILN_150 GBV_ILN_154 GBV_ILN_168 GBV_ILN_170 GBV_ILN_171 GBV_ILN_211 GBV_ILN_215 GBV_ILN_285 GBV_ILN_290 GBV_ILN_601 GBV_ILN_702 GBV_ILN_754 GBV_ILN_2002 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2008 GBV_ILN_2010 GBV_ILN_2012 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2016 GBV_ILN_2018 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2027 GBV_ILN_2095 GBV_ILN_2120 GBV_ILN_2121 GBV_ILN_2173 GBV_ILN_2190 GBV_ILN_2192 GBV_ILN_2219 GBV_ILN_2221 GBV_ILN_2279 GBV_ILN_2286 GBV_ILN_2360 GBV_ILN_2410 GBV_ILN_2411 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4046 GBV_ILN_4082 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4219 GBV_ILN_4277 GBV_ILN_4302 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4311 GBV_ILN_4314 GBV_ILN_4315 GBV_ILN_4317 GBV_ILN_4318 GBV_ILN_4320 GBV_ILN_4323 GBV_ILN_4385 GBV_ILN_4598 GBV_ILN_4700 AR 442 2006 7105 920-924 5
spelling	sw060825 (DE-627)OLC1723616915 (DE-599)GBVOLC1723616915 DE-627 ger DE-627 rakwb 070 500 500 AVZ BIODIV fid Cruts, Marc verfasserin aut Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21 2006 5 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier Gijselinck, Ilse oth van der Zee, Julie oth Engelborghs, Sebastiaan oth Wils, Hans oth Pirici, Daniel oth Rademakers, Rosa oth Vandenberghe, Rik oth Dermaut, Bart oth Martin, Jean-Jacques oth van Duijn, Cornelia oth Peeters, Karin oth Sciot, Raf oth Santens, Patrick oth De Pooter, Tim oth Mattheijssens, Maria oth Van den Broeck, Marleen oth Cuijt, Ivy oth Vennekens, Krist'l oth Enthalten in Nature London : Macmillan Publishers Limited, part of Springer Nature, 1869 442(2006), 7105, Seite 920-924 (DE-627)129292834 (DE-600)120714-3 (DE-576)014473941 0028-0836 nnns volume:442 year:2006 number:7105 pages:920-924 extent:5 GBV_USEFLAG_A SYSFLAG_A GBV_OLC FID-BIODIV SSG-OLC-PHY SSG-OLC-CHE SSG-OLC-MAT SSG-OLC-FOR SSG-OLC-SPO SSG-OLC-PHA SSG-OLC-DE-84 SSG-OPC-FOR GBV_ILN_11 GBV_ILN_20 GBV_ILN_21 GBV_ILN_22 GBV_ILN_23 GBV_ILN_30 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_47 GBV_ILN_55 GBV_ILN_59 GBV_ILN_60 GBV_ILN_62 GBV_ILN_69 GBV_ILN_70 GBV_ILN_95 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_130 GBV_ILN_150 GBV_ILN_154 GBV_ILN_168 GBV_ILN_170 GBV_ILN_171 GBV_ILN_211 GBV_ILN_215 GBV_ILN_285 GBV_ILN_290 GBV_ILN_601 GBV_ILN_702 GBV_ILN_754 GBV_ILN_2002 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2008 GBV_ILN_2010 GBV_ILN_2012 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2016 GBV_ILN_2018 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2027 GBV_ILN_2095 GBV_ILN_2120 GBV_ILN_2121 GBV_ILN_2173 GBV_ILN_2190 GBV_ILN_2192 GBV_ILN_2219 GBV_ILN_2221 GBV_ILN_2279 GBV_ILN_2286 GBV_ILN_2360 GBV_ILN_2410 GBV_ILN_2411 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4046 GBV_ILN_4082 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4219 GBV_ILN_4277 GBV_ILN_4302 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4311 GBV_ILN_4314 GBV_ILN_4315 GBV_ILN_4317 GBV_ILN_4318 GBV_ILN_4320 GBV_ILN_4323 GBV_ILN_4385 GBV_ILN_4598 GBV_ILN_4700 AR 442 2006 7105 920-924 5
allfields_unstemmed	sw060825 (DE-627)OLC1723616915 (DE-599)GBVOLC1723616915 DE-627 ger DE-627 rakwb 070 500 500 AVZ BIODIV fid Cruts, Marc verfasserin aut Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21 2006 5 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier Gijselinck, Ilse oth van der Zee, Julie oth Engelborghs, Sebastiaan oth Wils, Hans oth Pirici, Daniel oth Rademakers, Rosa oth Vandenberghe, Rik oth Dermaut, Bart oth Martin, Jean-Jacques oth van Duijn, Cornelia oth Peeters, Karin oth Sciot, Raf oth Santens, Patrick oth De Pooter, Tim oth Mattheijssens, Maria oth Van den Broeck, Marleen oth Cuijt, Ivy oth Vennekens, Krist'l oth Enthalten in Nature London : Macmillan Publishers Limited, part of Springer Nature, 1869 442(2006), 7105, Seite 920-924 (DE-627)129292834 (DE-600)120714-3 (DE-576)014473941 0028-0836 nnns volume:442 year:2006 number:7105 pages:920-924 extent:5 GBV_USEFLAG_A SYSFLAG_A GBV_OLC FID-BIODIV SSG-OLC-PHY SSG-OLC-CHE SSG-OLC-MAT SSG-OLC-FOR SSG-OLC-SPO SSG-OLC-PHA SSG-OLC-DE-84 SSG-OPC-FOR GBV_ILN_11 GBV_ILN_20 GBV_ILN_21 GBV_ILN_22 GBV_ILN_23 GBV_ILN_30 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_47 GBV_ILN_55 GBV_ILN_59 GBV_ILN_60 GBV_ILN_62 GBV_ILN_69 GBV_ILN_70 GBV_ILN_95 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_130 GBV_ILN_150 GBV_ILN_154 GBV_ILN_168 GBV_ILN_170 GBV_ILN_171 GBV_ILN_211 GBV_ILN_215 GBV_ILN_285 GBV_ILN_290 GBV_ILN_601 GBV_ILN_702 GBV_ILN_754 GBV_ILN_2002 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2008 GBV_ILN_2010 GBV_ILN_2012 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2016 GBV_ILN_2018 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2027 GBV_ILN_2095 GBV_ILN_2120 GBV_ILN_2121 GBV_ILN_2173 GBV_ILN_2190 GBV_ILN_2192 GBV_ILN_2219 GBV_ILN_2221 GBV_ILN_2279 GBV_ILN_2286 GBV_ILN_2360 GBV_ILN_2410 GBV_ILN_2411 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4046 GBV_ILN_4082 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4219 GBV_ILN_4277 GBV_ILN_4302 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4311 GBV_ILN_4314 GBV_ILN_4315 GBV_ILN_4317 GBV_ILN_4318 GBV_ILN_4320 GBV_ILN_4323 GBV_ILN_4385 GBV_ILN_4598 GBV_ILN_4700 AR 442 2006 7105 920-924 5
allfieldsGer	sw060825 (DE-627)OLC1723616915 (DE-599)GBVOLC1723616915 DE-627 ger DE-627 rakwb 070 500 500 AVZ BIODIV fid Cruts, Marc verfasserin aut Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21 2006 5 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier Gijselinck, Ilse oth van der Zee, Julie oth Engelborghs, Sebastiaan oth Wils, Hans oth Pirici, Daniel oth Rademakers, Rosa oth Vandenberghe, Rik oth Dermaut, Bart oth Martin, Jean-Jacques oth van Duijn, Cornelia oth Peeters, Karin oth Sciot, Raf oth Santens, Patrick oth De Pooter, Tim oth Mattheijssens, Maria oth Van den Broeck, Marleen oth Cuijt, Ivy oth Vennekens, Krist'l oth Enthalten in Nature London : Macmillan Publishers Limited, part of Springer Nature, 1869 442(2006), 7105, Seite 920-924 (DE-627)129292834 (DE-600)120714-3 (DE-576)014473941 0028-0836 nnns volume:442 year:2006 number:7105 pages:920-924 extent:5 GBV_USEFLAG_A SYSFLAG_A GBV_OLC FID-BIODIV SSG-OLC-PHY SSG-OLC-CHE SSG-OLC-MAT SSG-OLC-FOR SSG-OLC-SPO SSG-OLC-PHA SSG-OLC-DE-84 SSG-OPC-FOR GBV_ILN_11 GBV_ILN_20 GBV_ILN_21 GBV_ILN_22 GBV_ILN_23 GBV_ILN_30 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_47 GBV_ILN_55 GBV_ILN_59 GBV_ILN_60 GBV_ILN_62 GBV_ILN_69 GBV_ILN_70 GBV_ILN_95 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_130 GBV_ILN_150 GBV_ILN_154 GBV_ILN_168 GBV_ILN_170 GBV_ILN_171 GBV_ILN_211 GBV_ILN_215 GBV_ILN_285 GBV_ILN_290 GBV_ILN_601 GBV_ILN_702 GBV_ILN_754 GBV_ILN_2002 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2008 GBV_ILN_2010 GBV_ILN_2012 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2016 GBV_ILN_2018 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2027 GBV_ILN_2095 GBV_ILN_2120 GBV_ILN_2121 GBV_ILN_2173 GBV_ILN_2190 GBV_ILN_2192 GBV_ILN_2219 GBV_ILN_2221 GBV_ILN_2279 GBV_ILN_2286 GBV_ILN_2360 GBV_ILN_2410 GBV_ILN_2411 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4046 GBV_ILN_4082 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4219 GBV_ILN_4277 GBV_ILN_4302 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4311 GBV_ILN_4314 GBV_ILN_4315 GBV_ILN_4317 GBV_ILN_4318 GBV_ILN_4320 GBV_ILN_4323 GBV_ILN_4385 GBV_ILN_4598 GBV_ILN_4700 AR 442 2006 7105 920-924 5
allfieldsSound	sw060825 (DE-627)OLC1723616915 (DE-599)GBVOLC1723616915 DE-627 ger DE-627 rakwb 070 500 500 AVZ BIODIV fid Cruts, Marc verfasserin aut Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21 2006 5 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier Gijselinck, Ilse oth van der Zee, Julie oth Engelborghs, Sebastiaan oth Wils, Hans oth Pirici, Daniel oth Rademakers, Rosa oth Vandenberghe, Rik oth Dermaut, Bart oth Martin, Jean-Jacques oth van Duijn, Cornelia oth Peeters, Karin oth Sciot, Raf oth Santens, Patrick oth De Pooter, Tim oth Mattheijssens, Maria oth Van den Broeck, Marleen oth Cuijt, Ivy oth Vennekens, Krist'l oth Enthalten in Nature London : Macmillan Publishers Limited, part of Springer Nature, 1869 442(2006), 7105, Seite 920-924 (DE-627)129292834 (DE-600)120714-3 (DE-576)014473941 0028-0836 nnns volume:442 year:2006 number:7105 pages:920-924 extent:5 GBV_USEFLAG_A SYSFLAG_A GBV_OLC FID-BIODIV SSG-OLC-PHY SSG-OLC-CHE SSG-OLC-MAT SSG-OLC-FOR SSG-OLC-SPO SSG-OLC-PHA SSG-OLC-DE-84 SSG-OPC-FOR GBV_ILN_11 GBV_ILN_20 GBV_ILN_21 GBV_ILN_22 GBV_ILN_23 GBV_ILN_30 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_47 GBV_ILN_55 GBV_ILN_59 GBV_ILN_60 GBV_ILN_62 GBV_ILN_69 GBV_ILN_70 GBV_ILN_95 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_130 GBV_ILN_150 GBV_ILN_154 GBV_ILN_168 GBV_ILN_170 GBV_ILN_171 GBV_ILN_211 GBV_ILN_215 GBV_ILN_285 GBV_ILN_290 GBV_ILN_601 GBV_ILN_702 GBV_ILN_754 GBV_ILN_2002 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2008 GBV_ILN_2010 GBV_ILN_2012 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2016 GBV_ILN_2018 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2027 GBV_ILN_2095 GBV_ILN_2120 GBV_ILN_2121 GBV_ILN_2173 GBV_ILN_2190 GBV_ILN_2192 GBV_ILN_2219 GBV_ILN_2221 GBV_ILN_2279 GBV_ILN_2286 GBV_ILN_2360 GBV_ILN_2410 GBV_ILN_2411 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4046 GBV_ILN_4082 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4219 GBV_ILN_4277 GBV_ILN_4302 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4311 GBV_ILN_4314 GBV_ILN_4315 GBV_ILN_4317 GBV_ILN_4318 GBV_ILN_4320 GBV_ILN_4323 GBV_ILN_4385 GBV_ILN_4598 GBV_ILN_4700 AR 442 2006 7105 920-924 5
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title	Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21
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title_full	Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21
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title_sort	null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21
title_auth	Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21
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title_short	Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21
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author2	Gijselinck, Ilse van der Zee, Julie Engelborghs, Sebastiaan Wils, Hans Pirici, Daniel Rademakers, Rosa Vandenberghe, Rik Dermaut, Bart Martin, Jean-Jacques van Duijn, Cornelia Peeters, Karin Sciot, Raf Santens, Patrick De Pooter, Tim Mattheijssens, Maria Van den Broeck, Marleen Cuijt, Ivy Vennekens, Krist'l
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Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21

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