A novel central nervous system-enriched spinocerebellar ataxia type 7 gene product
- Author
- EINUM, David D1 ; CLARK, Anna M2 ; TOWNSEND, Jeannette J3 ; PTACEK, Louis J1 2 4 ; FU, Ying-Hui5
[1] Department of Human Genetics, University of Utah, Salt Lake City, United States
[2] Howard Hughes Medical Institute, University of Utah, Salt Lake City, United States
[3] Department of Pathology, University of Utah, Salt Lake City, United States
[4] Department of Neurology, University of Utah, Salt Lake City, United States
[5] Department of Neurology, University of California-San Francisco, United States - Source
Archives of neurology (Chicago). 2003, Vol 60, Num 1, pp 97-103, 7 p ; ref : 38 ref
- Publisher
- American Medical Association, Chicago, IL
- Publication country
- United States
- Document type
- Article
- Language
- English
- Keyword (fr)
- Ataxie spinocérébelleuse Déterminisme génétique Expression génique Gène Homme Immunohistochimie Phénotype Répartition spatiale Variant Ataxine Isoforme Anatomopathologie Appareil circulatoire pathologie Biologie moléculaire Encéphale pathologie Maladie dégénérative Maladie héréditaire Système nerveux central pathologie Système nerveux pathologie Vaisseau sanguin pathologie
- Keyword (en)
- Spinocerebellar ataxia Genetic determinism Gene expression Gene Human Immunohistochemistry Phenotype Spatial distribution Variant Ataxin Isoform Pathology Cardiovascular disease Molecular biology Cerebral disorder Degenerative disease Genetic disease Central nervous system disease Nervous system diseases Vascular disease
- Keyword (es)
- Ataxia spinocerebelosa Determinismo genético Expresión genética Gen Hombre Inmunohistoquímica Fenotipo Distribución espacial Variante Anatomía patológica Aparato circulatorio patología Biología molecular Encéfalo patología Enfermedad degenerativa Enfermedad hereditaria Sistema nervosio central patología Sistema nervioso patología Vaso sanguíneo patología
- Classification
- 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
- Neurology
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 14497543
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
10.1001/archneur.60.1.97 
https://dx.doi.org/10.1001/archneur.60.1.97
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