Variants in TSPYL1 are not associated with sudden infant death syndrome in a cohort of deceased infants from Switzerland
Sudden infant death syndrome (SIDS) is currently the major cause of an unexpected and unexplained death of infants in the first year of lifetime in industrialized countries. Besides environmental factors also genetic factors have been identified as risk factors for SIDS. Notably, the mutation c.457d...
Ausführliche Beschreibung
Gespeichert in:
| Autor*in: |
Schubert, Stephanie [verfasserIn] |
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E-Artikel |
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| Sprache: |
Englisch |
| Erschienen: |
2015transfer abstract |
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| Schlagwörter: |
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| Umfang: |
4 |
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| Übergeordnetes Werk: |
Enthalten in: Metamorphic - Xu, Nanqing ELSEVIER, 2022, London |
|---|---|
| Übergeordnetes Werk: |
volume:29 ; year:2015 ; number:1 ; pages:31-34 ; extent:4 |
| Links: |
|---|
| DOI / URN: |
10.1016/j.mcp.2014.10.006 |
|---|
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| 245 | 1 | 0 | |a Variants in TSPYL1 are not associated with sudden infant death syndrome in a cohort of deceased infants from Switzerland |
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| 520 | |a Sudden infant death syndrome (SIDS) is currently the major cause of an unexpected and unexplained death of infants in the first year of lifetime in industrialized countries. Besides environmental factors also genetic factors have been identified as risk factors for SIDS. Notably, the mutation c.457dupG (p.Glu153Glyfs*17) in the TSPYL1 gene has been reported to cause autosomal recessive sudden infant death with dysgenesis of the testes syndrome (SIDDT) in an Old Order Amish community in Pennsylvania. The purpose of this study was to analyze whether variants of TSPYL1 are associated with the sudden infant death syndrome (SIDS) in the area of Europe from which the Amish descended. Mutation analysis of the entire TSPYL1 gene was performed in a cohort of 165 SIDS cases with mostly Swiss ethnic origin, in comparison to 163 German controls. | ||
| 520 | |a Sudden infant death syndrome (SIDS) is currently the major cause of an unexpected and unexplained death of infants in the first year of lifetime in industrialized countries. Besides environmental factors also genetic factors have been identified as risk factors for SIDS. Notably, the mutation c.457dupG (p.Glu153Glyfs*17) in the TSPYL1 gene has been reported to cause autosomal recessive sudden infant death with dysgenesis of the testes syndrome (SIDDT) in an Old Order Amish community in Pennsylvania. The purpose of this study was to analyze whether variants of TSPYL1 are associated with the sudden infant death syndrome (SIDS) in the area of Europe from which the Amish descended. Mutation analysis of the entire TSPYL1 gene was performed in a cohort of 165 SIDS cases with mostly Swiss ethnic origin, in comparison to 163 German controls. | ||
| 650 | 7 | |a SIDS |2 Elsevier | |
| 650 | 7 | |a Genetic risk factors |2 Elsevier | |
| 650 | 7 | |a Mutation analysis |2 Elsevier | |
| 650 | 7 | |a TSPYL1 |2 Elsevier | |
| 700 | 1 | |a Haas, Cordula |4 oth | |
| 700 | 1 | |a Bartsch, Christine |4 oth | |
| 700 | 1 | |a Mirshekarnejad, Mandana |4 oth | |
| 700 | 1 | |a Kohrs, Sarah |4 oth | |
| 700 | 1 | |a Roettinger, Irene |4 oth | |
| 700 | 1 | |a Grosshennig, Anika |4 oth | |
| 700 | 1 | |a Stuhrmann, Manfred |4 oth | |
| 700 | 1 | |a Scholz, Caroline |4 oth | |
| 700 | 1 | |a Schmidtke, Jörg |4 oth | |
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10.1016/j.mcp.2014.10.006 doi GBVA2015015000024.pica (DE-627)ELV039826171 (ELSEVIER)S0890-8508(14)00052-8 DE-627 ger DE-627 rakwb eng 570 610 570 DE-600 610 DE-600 550 VZ 38.25 bkl 38.30 bkl 38.32 bkl Schubert, Stephanie verfasserin aut Variants in TSPYL1 are not associated with sudden infant death syndrome in a cohort of deceased infants from Switzerland 2015transfer abstract 4 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Sudden infant death syndrome (SIDS) is currently the major cause of an unexpected and unexplained death of infants in the first year of lifetime in industrialized countries. Besides environmental factors also genetic factors have been identified as risk factors for SIDS. Notably, the mutation c.457dupG (p.Glu153Glyfs*17) in the TSPYL1 gene has been reported to cause autosomal recessive sudden infant death with dysgenesis of the testes syndrome (SIDDT) in an Old Order Amish community in Pennsylvania. The purpose of this study was to analyze whether variants of TSPYL1 are associated with the sudden infant death syndrome (SIDS) in the area of Europe from which the Amish descended. Mutation analysis of the entire TSPYL1 gene was performed in a cohort of 165 SIDS cases with mostly Swiss ethnic origin, in comparison to 163 German controls. Sudden infant death syndrome (SIDS) is currently the major cause of an unexpected and unexplained death of infants in the first year of lifetime in industrialized countries. Besides environmental factors also genetic factors have been identified as risk factors for SIDS. Notably, the mutation c.457dupG (p.Glu153Glyfs*17) in the TSPYL1 gene has been reported to cause autosomal recessive sudden infant death with dysgenesis of the testes syndrome (SIDDT) in an Old Order Amish community in Pennsylvania. The purpose of this study was to analyze whether variants of TSPYL1 are associated with the sudden infant death syndrome (SIDS) in the area of Europe from which the Amish descended. Mutation analysis of the entire TSPYL1 gene was performed in a cohort of 165 SIDS cases with mostly Swiss ethnic origin, in comparison to 163 German controls. SIDS Elsevier Genetic risk factors Elsevier Mutation analysis Elsevier TSPYL1 Elsevier Haas, Cordula oth Bartsch, Christine oth Mirshekarnejad, Mandana oth Kohrs, Sarah oth Roettinger, Irene oth Grosshennig, Anika oth Stuhrmann, Manfred oth Scholz, Caroline oth Schmidtke, Jörg oth Enthalten in Academic Press Xu, Nanqing ELSEVIER Metamorphic 2022 London (DE-627)ELV008152659 volume:29 year:2015 number:1 pages:31-34 extent:4 https://doi.org/10.1016/j.mcp.2014.10.006 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OPC-GGO 38.25 Petrologie: Allgemeines VZ 38.30 Mineralogie VZ 38.32 Geochemie VZ AR 29 2015 1 31-34 4 045F 570 |
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10.1016/j.mcp.2014.10.006 doi GBVA2015015000024.pica (DE-627)ELV039826171 (ELSEVIER)S0890-8508(14)00052-8 DE-627 ger DE-627 rakwb eng 570 610 570 DE-600 610 DE-600 550 VZ 38.25 bkl 38.30 bkl 38.32 bkl Schubert, Stephanie verfasserin aut Variants in TSPYL1 are not associated with sudden infant death syndrome in a cohort of deceased infants from Switzerland 2015transfer abstract 4 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Sudden infant death syndrome (SIDS) is currently the major cause of an unexpected and unexplained death of infants in the first year of lifetime in industrialized countries. Besides environmental factors also genetic factors have been identified as risk factors for SIDS. Notably, the mutation c.457dupG (p.Glu153Glyfs*17) in the TSPYL1 gene has been reported to cause autosomal recessive sudden infant death with dysgenesis of the testes syndrome (SIDDT) in an Old Order Amish community in Pennsylvania. The purpose of this study was to analyze whether variants of TSPYL1 are associated with the sudden infant death syndrome (SIDS) in the area of Europe from which the Amish descended. Mutation analysis of the entire TSPYL1 gene was performed in a cohort of 165 SIDS cases with mostly Swiss ethnic origin, in comparison to 163 German controls. Sudden infant death syndrome (SIDS) is currently the major cause of an unexpected and unexplained death of infants in the first year of lifetime in industrialized countries. Besides environmental factors also genetic factors have been identified as risk factors for SIDS. Notably, the mutation c.457dupG (p.Glu153Glyfs*17) in the TSPYL1 gene has been reported to cause autosomal recessive sudden infant death with dysgenesis of the testes syndrome (SIDDT) in an Old Order Amish community in Pennsylvania. The purpose of this study was to analyze whether variants of TSPYL1 are associated with the sudden infant death syndrome (SIDS) in the area of Europe from which the Amish descended. Mutation analysis of the entire TSPYL1 gene was performed in a cohort of 165 SIDS cases with mostly Swiss ethnic origin, in comparison to 163 German controls. SIDS Elsevier Genetic risk factors Elsevier Mutation analysis Elsevier TSPYL1 Elsevier Haas, Cordula oth Bartsch, Christine oth Mirshekarnejad, Mandana oth Kohrs, Sarah oth Roettinger, Irene oth Grosshennig, Anika oth Stuhrmann, Manfred oth Scholz, Caroline oth Schmidtke, Jörg oth Enthalten in Academic Press Xu, Nanqing ELSEVIER Metamorphic 2022 London (DE-627)ELV008152659 volume:29 year:2015 number:1 pages:31-34 extent:4 https://doi.org/10.1016/j.mcp.2014.10.006 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OPC-GGO 38.25 Petrologie: Allgemeines VZ 38.30 Mineralogie VZ 38.32 Geochemie VZ AR 29 2015 1 31-34 4 045F 570 |
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10.1016/j.mcp.2014.10.006 doi GBVA2015015000024.pica (DE-627)ELV039826171 (ELSEVIER)S0890-8508(14)00052-8 DE-627 ger DE-627 rakwb eng 570 610 570 DE-600 610 DE-600 550 VZ 38.25 bkl 38.30 bkl 38.32 bkl Schubert, Stephanie verfasserin aut Variants in TSPYL1 are not associated with sudden infant death syndrome in a cohort of deceased infants from Switzerland 2015transfer abstract 4 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Sudden infant death syndrome (SIDS) is currently the major cause of an unexpected and unexplained death of infants in the first year of lifetime in industrialized countries. Besides environmental factors also genetic factors have been identified as risk factors for SIDS. Notably, the mutation c.457dupG (p.Glu153Glyfs*17) in the TSPYL1 gene has been reported to cause autosomal recessive sudden infant death with dysgenesis of the testes syndrome (SIDDT) in an Old Order Amish community in Pennsylvania. The purpose of this study was to analyze whether variants of TSPYL1 are associated with the sudden infant death syndrome (SIDS) in the area of Europe from which the Amish descended. Mutation analysis of the entire TSPYL1 gene was performed in a cohort of 165 SIDS cases with mostly Swiss ethnic origin, in comparison to 163 German controls. Sudden infant death syndrome (SIDS) is currently the major cause of an unexpected and unexplained death of infants in the first year of lifetime in industrialized countries. Besides environmental factors also genetic factors have been identified as risk factors for SIDS. Notably, the mutation c.457dupG (p.Glu153Glyfs*17) in the TSPYL1 gene has been reported to cause autosomal recessive sudden infant death with dysgenesis of the testes syndrome (SIDDT) in an Old Order Amish community in Pennsylvania. The purpose of this study was to analyze whether variants of TSPYL1 are associated with the sudden infant death syndrome (SIDS) in the area of Europe from which the Amish descended. Mutation analysis of the entire TSPYL1 gene was performed in a cohort of 165 SIDS cases with mostly Swiss ethnic origin, in comparison to 163 German controls. SIDS Elsevier Genetic risk factors Elsevier Mutation analysis Elsevier TSPYL1 Elsevier Haas, Cordula oth Bartsch, Christine oth Mirshekarnejad, Mandana oth Kohrs, Sarah oth Roettinger, Irene oth Grosshennig, Anika oth Stuhrmann, Manfred oth Scholz, Caroline oth Schmidtke, Jörg oth Enthalten in Academic Press Xu, Nanqing ELSEVIER Metamorphic 2022 London (DE-627)ELV008152659 volume:29 year:2015 number:1 pages:31-34 extent:4 https://doi.org/10.1016/j.mcp.2014.10.006 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OPC-GGO 38.25 Petrologie: Allgemeines VZ 38.30 Mineralogie VZ 38.32 Geochemie VZ AR 29 2015 1 31-34 4 045F 570 |
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10.1016/j.mcp.2014.10.006 doi GBVA2015015000024.pica (DE-627)ELV039826171 (ELSEVIER)S0890-8508(14)00052-8 DE-627 ger DE-627 rakwb eng 570 610 570 DE-600 610 DE-600 550 VZ 38.25 bkl 38.30 bkl 38.32 bkl Schubert, Stephanie verfasserin aut Variants in TSPYL1 are not associated with sudden infant death syndrome in a cohort of deceased infants from Switzerland 2015transfer abstract 4 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Sudden infant death syndrome (SIDS) is currently the major cause of an unexpected and unexplained death of infants in the first year of lifetime in industrialized countries. Besides environmental factors also genetic factors have been identified as risk factors for SIDS. Notably, the mutation c.457dupG (p.Glu153Glyfs*17) in the TSPYL1 gene has been reported to cause autosomal recessive sudden infant death with dysgenesis of the testes syndrome (SIDDT) in an Old Order Amish community in Pennsylvania. The purpose of this study was to analyze whether variants of TSPYL1 are associated with the sudden infant death syndrome (SIDS) in the area of Europe from which the Amish descended. Mutation analysis of the entire TSPYL1 gene was performed in a cohort of 165 SIDS cases with mostly Swiss ethnic origin, in comparison to 163 German controls. Sudden infant death syndrome (SIDS) is currently the major cause of an unexpected and unexplained death of infants in the first year of lifetime in industrialized countries. Besides environmental factors also genetic factors have been identified as risk factors for SIDS. Notably, the mutation c.457dupG (p.Glu153Glyfs*17) in the TSPYL1 gene has been reported to cause autosomal recessive sudden infant death with dysgenesis of the testes syndrome (SIDDT) in an Old Order Amish community in Pennsylvania. The purpose of this study was to analyze whether variants of TSPYL1 are associated with the sudden infant death syndrome (SIDS) in the area of Europe from which the Amish descended. Mutation analysis of the entire TSPYL1 gene was performed in a cohort of 165 SIDS cases with mostly Swiss ethnic origin, in comparison to 163 German controls. SIDS Elsevier Genetic risk factors Elsevier Mutation analysis Elsevier TSPYL1 Elsevier Haas, Cordula oth Bartsch, Christine oth Mirshekarnejad, Mandana oth Kohrs, Sarah oth Roettinger, Irene oth Grosshennig, Anika oth Stuhrmann, Manfred oth Scholz, Caroline oth Schmidtke, Jörg oth Enthalten in Academic Press Xu, Nanqing ELSEVIER Metamorphic 2022 London (DE-627)ELV008152659 volume:29 year:2015 number:1 pages:31-34 extent:4 https://doi.org/10.1016/j.mcp.2014.10.006 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OPC-GGO 38.25 Petrologie: Allgemeines VZ 38.30 Mineralogie VZ 38.32 Geochemie VZ AR 29 2015 1 31-34 4 045F 570 |
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10.1016/j.mcp.2014.10.006 doi GBVA2015015000024.pica (DE-627)ELV039826171 (ELSEVIER)S0890-8508(14)00052-8 DE-627 ger DE-627 rakwb eng 570 610 570 DE-600 610 DE-600 550 VZ 38.25 bkl 38.30 bkl 38.32 bkl Schubert, Stephanie verfasserin aut Variants in TSPYL1 are not associated with sudden infant death syndrome in a cohort of deceased infants from Switzerland 2015transfer abstract 4 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Sudden infant death syndrome (SIDS) is currently the major cause of an unexpected and unexplained death of infants in the first year of lifetime in industrialized countries. Besides environmental factors also genetic factors have been identified as risk factors for SIDS. Notably, the mutation c.457dupG (p.Glu153Glyfs*17) in the TSPYL1 gene has been reported to cause autosomal recessive sudden infant death with dysgenesis of the testes syndrome (SIDDT) in an Old Order Amish community in Pennsylvania. The purpose of this study was to analyze whether variants of TSPYL1 are associated with the sudden infant death syndrome (SIDS) in the area of Europe from which the Amish descended. Mutation analysis of the entire TSPYL1 gene was performed in a cohort of 165 SIDS cases with mostly Swiss ethnic origin, in comparison to 163 German controls. Sudden infant death syndrome (SIDS) is currently the major cause of an unexpected and unexplained death of infants in the first year of lifetime in industrialized countries. Besides environmental factors also genetic factors have been identified as risk factors for SIDS. Notably, the mutation c.457dupG (p.Glu153Glyfs*17) in the TSPYL1 gene has been reported to cause autosomal recessive sudden infant death with dysgenesis of the testes syndrome (SIDDT) in an Old Order Amish community in Pennsylvania. The purpose of this study was to analyze whether variants of TSPYL1 are associated with the sudden infant death syndrome (SIDS) in the area of Europe from which the Amish descended. Mutation analysis of the entire TSPYL1 gene was performed in a cohort of 165 SIDS cases with mostly Swiss ethnic origin, in comparison to 163 German controls. SIDS Elsevier Genetic risk factors Elsevier Mutation analysis Elsevier TSPYL1 Elsevier Haas, Cordula oth Bartsch, Christine oth Mirshekarnejad, Mandana oth Kohrs, Sarah oth Roettinger, Irene oth Grosshennig, Anika oth Stuhrmann, Manfred oth Scholz, Caroline oth Schmidtke, Jörg oth Enthalten in Academic Press Xu, Nanqing ELSEVIER Metamorphic 2022 London (DE-627)ELV008152659 volume:29 year:2015 number:1 pages:31-34 extent:4 https://doi.org/10.1016/j.mcp.2014.10.006 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OPC-GGO 38.25 Petrologie: Allgemeines VZ 38.30 Mineralogie VZ 38.32 Geochemie VZ AR 29 2015 1 31-34 4 045F 570 |
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Variants in TSPYL1 are not associated with sudden infant death syndrome in a cohort of deceased infants from Switzerland |
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Sudden infant death syndrome (SIDS) is currently the major cause of an unexpected and unexplained death of infants in the first year of lifetime in industrialized countries. Besides environmental factors also genetic factors have been identified as risk factors for SIDS. Notably, the mutation c.457dupG (p.Glu153Glyfs*17) in the TSPYL1 gene has been reported to cause autosomal recessive sudden infant death with dysgenesis of the testes syndrome (SIDDT) in an Old Order Amish community in Pennsylvania. The purpose of this study was to analyze whether variants of TSPYL1 are associated with the sudden infant death syndrome (SIDS) in the area of Europe from which the Amish descended. Mutation analysis of the entire TSPYL1 gene was performed in a cohort of 165 SIDS cases with mostly Swiss ethnic origin, in comparison to 163 German controls. |
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Sudden infant death syndrome (SIDS) is currently the major cause of an unexpected and unexplained death of infants in the first year of lifetime in industrialized countries. Besides environmental factors also genetic factors have been identified as risk factors for SIDS. Notably, the mutation c.457dupG (p.Glu153Glyfs*17) in the TSPYL1 gene has been reported to cause autosomal recessive sudden infant death with dysgenesis of the testes syndrome (SIDDT) in an Old Order Amish community in Pennsylvania. The purpose of this study was to analyze whether variants of TSPYL1 are associated with the sudden infant death syndrome (SIDS) in the area of Europe from which the Amish descended. Mutation analysis of the entire TSPYL1 gene was performed in a cohort of 165 SIDS cases with mostly Swiss ethnic origin, in comparison to 163 German controls. |
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Sudden infant death syndrome (SIDS) is currently the major cause of an unexpected and unexplained death of infants in the first year of lifetime in industrialized countries. Besides environmental factors also genetic factors have been identified as risk factors for SIDS. Notably, the mutation c.457dupG (p.Glu153Glyfs*17) in the TSPYL1 gene has been reported to cause autosomal recessive sudden infant death with dysgenesis of the testes syndrome (SIDDT) in an Old Order Amish community in Pennsylvania. The purpose of this study was to analyze whether variants of TSPYL1 are associated with the sudden infant death syndrome (SIDS) in the area of Europe from which the Amish descended. Mutation analysis of the entire TSPYL1 gene was performed in a cohort of 165 SIDS cases with mostly Swiss ethnic origin, in comparison to 163 German controls. |
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