TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis
- Author
- KABASHI, Edor1 ; VALDMANIS, Paul N1 ; PRADAT, Pierre-Francois4 ; CAMU, William5 ; MEININGER, Vincent4 ; DUPRE, Nicolas1 3 ; ROULEAU, Guy A1 ; DION, Patrick1 ; SPIEGELMAN, Dan1 ; MCCONKEY, Brendan J2 ; VANDE VELDE, Christine1 ; BOUCHARD, Jean-Pierre3 ; LACOMBLEZ, Lucette4 ; POCHIGAEVA, Ksenia4 ; SALACHAS, Francois4
[1] Center of Excellence in Neuromics, Centre Hospitalier de l'Universite de Montreal, and Department of Medicine, University of Montreal, Montreal, Quebec H2L4M1, Canada
[2] Department of Biology, University of Waterloo, 200 University Avenue West, Waterloo, Ontario N2L 3G1, Canada
[3] Faculty of Medicine, Laval University, Centre Hospitalier Affilié Universitaire de Québec -Enfant-Jesus Hospital, Quebec G1J1Z4, Canada
[4] Fédération des maladies du système nerveux, Division Paul Castaigne, Hôpital de la Salpêtrière, Paris 75651, France
[5] Unité de Neurologie Comportementale et Dégénérative, Institute of Biology, Montpellier 34967, France - Source
Nature genetics. 2008, Vol 40, Num 5, pp 572-574, 3 p ; ref : 15 ref
- Publisher
- Nature Publishing Group, London
- Publication country
- United Kingdom
- Document type
- Article
- Language
- English
- Keyword (fr)
- Mutation Sclérose latérale amyotrophique Sporadique Maladie dégénérative Pathologie de la moelle épinière Pathologie du système nerveux central Pathologie du système nerveux
- Keyword (en)
- Mutation Amyotrophic lateral sclerosis Sporadic Degenerative disease Spinal cord disease Central nervous system disease Nervous system diseases
- Keyword (es)
- Mutación Esclerosis lateral amiotrófica Esporádico Enfermedad degenerativa Médula espinal patología Sistema nervosio central patología Sistema nervioso patología
- Classification
- Pascal
- 002 Biological and medical sciences / 002A Fundamental and applied biological sciences. Psychology / 002A07 Genetics of eukaryotes. Biological and molecular evolution
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B17 Neurology / 002B17A Nervous system (semeiology, syndromes) / 002B17A07 Cerebrospinal fluid. Meninges. Spinal cord
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B17 Neurology / 002B17G Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases
- Discipline
- Eukaryotes genetics. Biological and molecular evolution Neurology
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 20329973
Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS
Access to the document
Install on your browser
DOI
10.1038/ng.132 
https://dx.doi.org/10.1038/ng.132
"O:13:\"PanistOpenUrl\":36:{s:10:\"\u0000*\u0000openUrl\";N;s:6:\"\u0000*\u0000idc\";N;s:6:\"\u0000*\u0000fmt\";s:7:\"journal\";s:6:\"\u0000*\u0000doi\";s:14:\"10.1038\/ng.132\";s:6:\"\u0000*\u0000pii\";s:0:\"\";s:7:\"\u0000*\u0000pmid\";s:0:\"\";s:9:\"\u0000*\u0000atitle\";s:88:\"TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis\";s:9:\"\u0000*\u0000jtitle\";s:15:\"Nature genetics\";s:9:\"\u0000*\u0000stitle\";s:10:\"Nat. genet\";s:7:\"\u0000*\u0000date\";s:4:\"2008\";s:9:\"\u0000*\u0000volume\";s:2:\"40\";s:8:\"\u0000*\u0000issue\";s:1:\"5\";s:8:\"\u0000*\u0000spage\";s:3:\"572\";s:8:\"\u0000*\u0000epage\";s:3:\"574\";s:8:\"\u0000*\u0000pages\";s:0:\"\";s:7:\"\u0000*\u0000issn\";s:9:\"1061-4036\";s:8:\"\u0000*\u0000eissn\";s:0:\"\";s:9:\"\u0000*\u0000aulast\";s:7:\"KABASHI\";s:10:\"\u0000*\u0000aufirst\";s:4:\"Edor\";s:9:\"\u0000*\u0000auinit\";s:0:\"\";s:10:\"\u0000*\u0000auinitm\";s:0:\"\";s:5:\"\u0000*\u0000au\";a:14:{i:0;s:17:\"VALDMANIS, Paul N\";i:1;s:23:\"PRADAT, Pierre-Francois\";i:2;s:13:\"CAMU, William\";i:3;s:18:\"MEININGER, Vincent\";i:4;s:14:\"DUPRE, Nicolas\";i:5;s:14:\"ROULEAU, Guy A\";i:6;s:13:\"DION, Patrick\";i:7;s:15:\"SPIEGELMAN, Dan\";i:8;s:19:\"MCCONKEY, Brendan J\";i:9;s:22:\"VANDE VELDE, Christine\";i:10;s:21:\"BOUCHARD, Jean-Pierre\";i:11;s:18:\"LACOMBLEZ, Lucette\";i:12;s:18:\"POCHIGAEVA, Ksenia\";i:13;s:18:\"SALACHAS, Francois\";}s:9:\"\u0000*\u0000aucorp\";s:0:\"\";s:7:\"\u0000*\u0000isbn\";s:0:\"\";s:8:\"\u0000*\u0000coden\";s:6:\"NGENEC\";s:8:\"\u0000*\u0000genre\";s:7:\"article\";s:7:\"\u0000*\u0000part\";s:0:\"\";s:9:\"\u0000*\u0000btitle\";s:0:\"\";s:8:\"\u0000*\u0000title\";s:88:\"TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis\";s:8:\"\u0000*\u0000place\";s:6:\"London\";s:6:\"\u0000*\u0000pub\";s:23:\"Nature Publishing Group\";s:10:\"\u0000*\u0000edition\";s:0:\"\";s:9:\"\u0000*\u0000tpages\";s:1:\"3\";s:9:\"\u0000*\u0000series\";s:0:\"\";s:8:\"\u0000*\u0000proxy\";s:30:\"http:\/\/proxyout.inist.fr:8080\/\";s:12:\"\u0000*\u0000integrite\";b:1;}"
Panist access
"O:12:\"IstexOpenUrl\":35:{s:10:\"\u0000*\u0000openUrl\";N;s:6:\"\u0000*\u0000fmt\";s:7:\"journal\";s:6:\"\u0000*\u0000doi\";s:14:\"10.1038\/ng.132\";s:6:\"\u0000*\u0000pii\";s:0:\"\";s:7:\"\u0000*\u0000pmid\";s:0:\"\";s:9:\"\u0000*\u0000atitle\";s:88:\"TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis\";s:9:\"\u0000*\u0000jtitle\";s:15:\"Nature genetics\";s:9:\"\u0000*\u0000stitle\";s:10:\"Nat. genet\";s:7:\"\u0000*\u0000date\";s:4:\"2008\";s:9:\"\u0000*\u0000volume\";s:2:\"40\";s:8:\"\u0000*\u0000issue\";s:1:\"5\";s:8:\"\u0000*\u0000spage\";s:3:\"572\";s:8:\"\u0000*\u0000epage\";s:3:\"574\";s:8:\"\u0000*\u0000pages\";s:0:\"\";s:7:\"\u0000*\u0000issn\";s:9:\"1061-4036\";s:8:\"\u0000*\u0000eissn\";s:0:\"\";s:9:\"\u0000*\u0000aulast\";s:7:\"KABASHI\";s:10:\"\u0000*\u0000aufirst\";s:4:\"Edor\";s:9:\"\u0000*\u0000auinit\";s:0:\"\";s:10:\"\u0000*\u0000auinitm\";s:0:\"\";s:5:\"\u0000*\u0000au\";a:14:{i:0;s:17:\"VALDMANIS, Paul N\";i:1;s:23:\"PRADAT, Pierre-Francois\";i:2;s:13:\"CAMU, William\";i:3;s:18:\"MEININGER, Vincent\";i:4;s:14:\"DUPRE, Nicolas\";i:5;s:14:\"ROULEAU, Guy A\";i:6;s:13:\"DION, Patrick\";i:7;s:15:\"SPIEGELMAN, Dan\";i:8;s:19:\"MCCONKEY, Brendan J\";i:9;s:22:\"VANDE VELDE, Christine\";i:10;s:21:\"BOUCHARD, Jean-Pierre\";i:11;s:18:\"LACOMBLEZ, Lucette\";i:12;s:18:\"POCHIGAEVA, Ksenia\";i:13;s:18:\"SALACHAS, Francois\";}s:9:\"\u0000*\u0000aucorp\";s:0:\"\";s:7:\"\u0000*\u0000isbn\";s:0:\"\";s:8:\"\u0000*\u0000coden\";s:6:\"NGENEC\";s:8:\"\u0000*\u0000genre\";s:7:\"article\";s:7:\"\u0000*\u0000part\";s:0:\"\";s:9:\"\u0000*\u0000btitle\";s:0:\"\";s:8:\"\u0000*\u0000title\";s:88:\"TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis\";s:8:\"\u0000*\u0000place\";s:6:\"London\";s:6:\"\u0000*\u0000pub\";s:23:\"Nature Publishing Group\";s:10:\"\u0000*\u0000edition\";s:0:\"\";s:9:\"\u0000*\u0000tpages\";s:1:\"3\";s:9:\"\u0000*\u0000series\";s:0:\"\";s:8:\"\u0000*\u0000proxy\";s:30:\"http:\/\/proxyout.inist.fr:8080\/\";s:12:\"\u0000*\u0000integrite\";b:1;}"
Istex access
"O:16:\"UnpaywallOpenUrl\":35:{s:8:\"\u0000*\u0000email\";s:27:\"assistance-portail@inist.fr\";s:6:\"\u0000*\u0000fmt\";N;s:6:\"\u0000*\u0000doi\";s:14:\"10.1038\/ng.132\";s:6:\"\u0000*\u0000pii\";N;s:7:\"\u0000*\u0000pmid\";N;s:9:\"\u0000*\u0000atitle\";N;s:9:\"\u0000*\u0000jtitle\";N;s:9:\"\u0000*\u0000stitle\";N;s:7:\"\u0000*\u0000date\";N;s:9:\"\u0000*\u0000volume\";N;s:8:\"\u0000*\u0000issue\";N;s:8:\"\u0000*\u0000spage\";N;s:8:\"\u0000*\u0000epage\";N;s:8:\"\u0000*\u0000pages\";N;s:7:\"\u0000*\u0000issn\";N;s:8:\"\u0000*\u0000eissn\";N;s:9:\"\u0000*\u0000aulast\";N;s:10:\"\u0000*\u0000aufirst\";N;s:9:\"\u0000*\u0000auinit\";N;s:10:\"\u0000*\u0000auinitm\";N;s:5:\"\u0000*\u0000au\";N;s:9:\"\u0000*\u0000aucorp\";N;s:7:\"\u0000*\u0000isbn\";N;s:8:\"\u0000*\u0000coden\";N;s:8:\"\u0000*\u0000genre\";N;s:7:\"\u0000*\u0000part\";N;s:9:\"\u0000*\u0000btitle\";N;s:8:\"\u0000*\u0000title\";N;s:8:\"\u0000*\u0000place\";N;s:6:\"\u0000*\u0000pub\";N;s:10:\"\u0000*\u0000edition\";N;s:9:\"\u0000*\u0000tpages\";N;s:9:\"\u0000*\u0000series\";N;s:8:\"\u0000*\u0000proxy\";s:30:\"http:\/\/proxyout.inist.fr:8080\/\";s:12:\"\u0000*\u0000integrite\";N;}"
Unpaywall access
"O:16:\"EuropePMCOpenUrl\":35:{s:10:\"\u0000*\u0000openUrl\";N;s:6:\"\u0000*\u0000fmt\";s:7:\"journal\";s:6:\"\u0000*\u0000doi\";s:14:\"10.1038\/ng.132\";s:6:\"\u0000*\u0000pii\";s:0:\"\";s:7:\"\u0000*\u0000pmid\";s:0:\"\";s:9:\"\u0000*\u0000atitle\";s:88:\"TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis\";s:9:\"\u0000*\u0000jtitle\";s:15:\"Nature genetics\";s:9:\"\u0000*\u0000stitle\";s:10:\"Nat. genet\";s:7:\"\u0000*\u0000date\";s:4:\"2008\";s:9:\"\u0000*\u0000volume\";s:2:\"40\";s:8:\"\u0000*\u0000issue\";s:1:\"5\";s:8:\"\u0000*\u0000spage\";s:3:\"572\";s:8:\"\u0000*\u0000epage\";s:3:\"574\";s:8:\"\u0000*\u0000pages\";s:0:\"\";s:7:\"\u0000*\u0000issn\";s:9:\"1061-4036\";s:8:\"\u0000*\u0000eissn\";s:0:\"\";s:9:\"\u0000*\u0000aulast\";s:7:\"KABASHI\";s:10:\"\u0000*\u0000aufirst\";s:4:\"Edor\";s:9:\"\u0000*\u0000auinit\";s:0:\"\";s:10:\"\u0000*\u0000auinitm\";s:0:\"\";s:5:\"\u0000*\u0000au\";a:14:{i:0;s:17:\"VALDMANIS, Paul N\";i:1;s:23:\"PRADAT, Pierre-Francois\";i:2;s:13:\"CAMU, William\";i:3;s:18:\"MEININGER, Vincent\";i:4;s:14:\"DUPRE, Nicolas\";i:5;s:14:\"ROULEAU, Guy A\";i:6;s:13:\"DION, Patrick\";i:7;s:15:\"SPIEGELMAN, Dan\";i:8;s:19:\"MCCONKEY, Brendan J\";i:9;s:22:\"VANDE VELDE, Christine\";i:10;s:21:\"BOUCHARD, Jean-Pierre\";i:11;s:18:\"LACOMBLEZ, Lucette\";i:12;s:18:\"POCHIGAEVA, Ksenia\";i:13;s:18:\"SALACHAS, Francois\";}s:9:\"\u0000*\u0000aucorp\";s:0:\"\";s:7:\"\u0000*\u0000isbn\";s:0:\"\";s:8:\"\u0000*\u0000coden\";s:6:\"NGENEC\";s:8:\"\u0000*\u0000genre\";s:7:\"article\";s:7:\"\u0000*\u0000part\";s:0:\"\";s:9:\"\u0000*\u0000btitle\";s:0:\"\";s:8:\"\u0000*\u0000title\";s:88:\"TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis\";s:8:\"\u0000*\u0000place\";s:6:\"London\";s:6:\"\u0000*\u0000pub\";s:23:\"Nature Publishing Group\";s:10:\"\u0000*\u0000edition\";s:0:\"\";s:9:\"\u0000*\u0000tpages\";s:1:\"3\";s:9:\"\u0000*\u0000series\";s:0:\"\";s:8:\"\u0000*\u0000proxy\";s:30:\"http:\/\/proxyout.inist.fr:8080\/\";s:12:\"\u0000*\u0000integrite\";b:1;}"
Europe PubMed Central access
"O:11:\"BaseOpenUrl\":35:{s:10:\"\u0000*\u0000openUrl\";N;s:6:\"\u0000*\u0000fmt\";s:7:\"journal\";s:6:\"\u0000*\u0000doi\";s:14:\"10.1038\/ng.132\";s:6:\"\u0000*\u0000pii\";s:0:\"\";s:7:\"\u0000*\u0000pmid\";s:0:\"\";s:9:\"\u0000*\u0000atitle\";s:88:\"TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis\";s:9:\"\u0000*\u0000jtitle\";s:15:\"Nature genetics\";s:9:\"\u0000*\u0000stitle\";s:10:\"Nat. genet\";s:7:\"\u0000*\u0000date\";s:4:\"2008\";s:9:\"\u0000*\u0000volume\";s:2:\"40\";s:8:\"\u0000*\u0000issue\";s:1:\"5\";s:8:\"\u0000*\u0000spage\";s:3:\"572\";s:8:\"\u0000*\u0000epage\";s:3:\"574\";s:8:\"\u0000*\u0000pages\";s:0:\"\";s:7:\"\u0000*\u0000issn\";s:9:\"1061-4036\";s:8:\"\u0000*\u0000eissn\";s:0:\"\";s:9:\"\u0000*\u0000aulast\";s:7:\"KABASHI\";s:10:\"\u0000*\u0000aufirst\";s:4:\"Edor\";s:9:\"\u0000*\u0000auinit\";s:0:\"\";s:10:\"\u0000*\u0000auinitm\";s:0:\"\";s:5:\"\u0000*\u0000au\";a:14:{i:0;s:17:\"VALDMANIS, Paul N\";i:1;s:23:\"PRADAT, Pierre-Francois\";i:2;s:13:\"CAMU, William\";i:3;s:18:\"MEININGER, Vincent\";i:4;s:14:\"DUPRE, Nicolas\";i:5;s:14:\"ROULEAU, Guy A\";i:6;s:13:\"DION, Patrick\";i:7;s:15:\"SPIEGELMAN, Dan\";i:8;s:19:\"MCCONKEY, Brendan J\";i:9;s:22:\"VANDE VELDE, Christine\";i:10;s:21:\"BOUCHARD, Jean-Pierre\";i:11;s:18:\"LACOMBLEZ, Lucette\";i:12;s:18:\"POCHIGAEVA, Ksenia\";i:13;s:18:\"SALACHAS, Francois\";}s:9:\"\u0000*\u0000aucorp\";s:0:\"\";s:7:\"\u0000*\u0000isbn\";s:0:\"\";s:8:\"\u0000*\u0000coden\";s:6:\"NGENEC\";s:8:\"\u0000*\u0000genre\";s:7:\"article\";s:7:\"\u0000*\u0000part\";s:0:\"\";s:9:\"\u0000*\u0000btitle\";s:0:\"\";s:8:\"\u0000*\u0000title\";s:88:\"TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis\";s:8:\"\u0000*\u0000place\";s:6:\"London\";s:6:\"\u0000*\u0000pub\";s:23:\"Nature Publishing Group\";s:10:\"\u0000*\u0000edition\";s:0:\"\";s:9:\"\u0000*\u0000tpages\";s:1:\"3\";s:9:\"\u0000*\u0000series\";s:0:\"\";s:8:\"\u0000*\u0000proxy\";s:30:\"http:\/\/proxyout.inist.fr:8080\/\";s:12:\"\u0000*\u0000integrite\";b:1;}"
Base Search access
"O:12:\"ArXivOpenUrl\":35:{s:10:\"\u0000*\u0000openUrl\";N;s:6:\"\u0000*\u0000fmt\";s:7:\"journal\";s:6:\"\u0000*\u0000doi\";s:14:\"10.1038\/ng.132\";s:6:\"\u0000*\u0000pii\";s:0:\"\";s:7:\"\u0000*\u0000pmid\";s:0:\"\";s:9:\"\u0000*\u0000atitle\";s:88:\"TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis\";s:9:\"\u0000*\u0000jtitle\";s:15:\"Nature genetics\";s:9:\"\u0000*\u0000stitle\";s:10:\"Nat. genet\";s:7:\"\u0000*\u0000date\";s:4:\"2008\";s:9:\"\u0000*\u0000volume\";s:2:\"40\";s:8:\"\u0000*\u0000issue\";s:1:\"5\";s:8:\"\u0000*\u0000spage\";s:3:\"572\";s:8:\"\u0000*\u0000epage\";s:3:\"574\";s:8:\"\u0000*\u0000pages\";s:0:\"\";s:7:\"\u0000*\u0000issn\";s:9:\"1061-4036\";s:8:\"\u0000*\u0000eissn\";s:0:\"\";s:9:\"\u0000*\u0000aulast\";s:7:\"KABASHI\";s:10:\"\u0000*\u0000aufirst\";s:4:\"Edor\";s:9:\"\u0000*\u0000auinit\";s:0:\"\";s:10:\"\u0000*\u0000auinitm\";s:0:\"\";s:5:\"\u0000*\u0000au\";a:14:{i:0;s:17:\"VALDMANIS, Paul N\";i:1;s:23:\"PRADAT, Pierre-Francois\";i:2;s:13:\"CAMU, William\";i:3;s:18:\"MEININGER, Vincent\";i:4;s:14:\"DUPRE, Nicolas\";i:5;s:14:\"ROULEAU, Guy A\";i:6;s:13:\"DION, Patrick\";i:7;s:15:\"SPIEGELMAN, Dan\";i:8;s:19:\"MCCONKEY, Brendan J\";i:9;s:22:\"VANDE VELDE, Christine\";i:10;s:21:\"BOUCHARD, Jean-Pierre\";i:11;s:18:\"LACOMBLEZ, Lucette\";i:12;s:18:\"POCHIGAEVA, Ksenia\";i:13;s:18:\"SALACHAS, Francois\";}s:9:\"\u0000*\u0000aucorp\";s:0:\"\";s:7:\"\u0000*\u0000isbn\";s:0:\"\";s:8:\"\u0000*\u0000coden\";s:6:\"NGENEC\";s:8:\"\u0000*\u0000genre\";s:7:\"article\";s:7:\"\u0000*\u0000part\";s:0:\"\";s:9:\"\u0000*\u0000btitle\";s:0:\"\";s:8:\"\u0000*\u0000title\";s:88:\"TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis\";s:8:\"\u0000*\u0000place\";s:6:\"London\";s:6:\"\u0000*\u0000pub\";s:23:\"Nature Publishing Group\";s:10:\"\u0000*\u0000edition\";s:0:\"\";s:9:\"\u0000*\u0000tpages\";s:1:\"3\";s:9:\"\u0000*\u0000series\";s:0:\"\";s:8:\"\u0000*\u0000proxy\";s:30:\"http:\/\/proxyout.inist.fr:8080\/\";s:12:\"\u0000*\u0000integrite\";b:1;}"
arXiv access
