Mutations in SYNE1 lead to a newly discovered form of autosomal recessive cerebellar ataxia
- Author
- GROS-LOUIS, Francois1 ; DUPRE, Nicolas1 2 ; DION, Patrick1 ; FOX, Michael A3 ; LAURENT, Sandra1 ; VERREAULT, Steve2 ; SANES, Joshua R3 ; BOUCHARD, Jean-Pierre2 ; ROULEAU, Guy A1
[1] Centre for the Study of Brain Diseases, Centre Hospitalier de l'Université de Montréal and Centre Hospitalier Universitaire -Ste-Justine, Université de Montréal, Montréal, Quebec, H2L4M1, Canada
[2] Faculty of Medicine, Laval University, Department of Neurological Sciences, Centre Hospitalier Affilié Universitaire de Québec -Enfant-Jesus Hospital, Quebec City, Quebec, G1J 1Z4, Canada
[3] Department of Molecular and Cellular Biology, Harvard University, Cambridge, Massachusetts 02138, United States - Source
Nature genetics. 2007, Vol 39, Num 1, pp 80-85, 6 p ; ref : 22 ref
- Publisher
- Nature Publishing Group, London
- Publication country
- United Kingdom
- Document type
- Article
- Language
- English
- Keyword (fr)
- Ataxie cérébelleuse Autosome Mutation
- Keyword (en)
- Cerebellar ataxia Autosome Mutation
- Keyword (es)
- Ataxia cerebelosa Autosoma Mutación
- Classification
- Pascal
- 002 Biological and medical sciences / 002A Fundamental and applied biological sciences. Psychology / 002A07 Genetics of eukaryotes. Biological and molecular evolution
- Discipline
- Eukaryotes genetics. Biological and molecular evolution
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 18572547
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
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DOI
10.1038/ng1927 
https://dx.doi.org/10.1038/ng1927
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