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Analysis of the SCA1 CAG repeat in a large number of families with dominant ataxia : clinical and molecular correlations

Author
DUBOURG, O1 ; DÜRR, A1 ; CANCEL, G1 ; STEVANIN, G1 ; CHNEIWEISS, H2 ; PENET, C1 ; AGID, Y1 ; BRICE, A1
[1] INSERM Hôp. Salpêtrière, U 289, 75651 Paris, France
[2] INSERM Coll. France, U 114, Paris, France
Source

Annals of neurology. 1995, Vol 37, Num 2, pp 176-180 ; ref : 29 ref

CODEN
ANNED3
ISSN
0364-5134
Scientific domain
Neurology
Publisher
Willey-Liss, Hoboken
Publication country
United Kingdom
Document type
Article
Language
English
Keyword (fr)
Déterminisme génétique Etude familiale Homme Hérédodégénérescence spinocérébelleuse Encéphale pathologie Maladie dégénérative Maladie héréditaire Moelle épinière pathologie Système nerveux central pathologie Système nerveux pathologie
Keyword (en)
Genetic inheritance Family study Human Spinocerebellar heredodegeneration Cerebral disorder Degenerative disease Genetic disease Spinal cord disease Central nervous system disease Nervous system diseases
Keyword (es)
Determinismo genético Estudio familiar Hombre Heredodegeneración espinocerebelosa Encéfalo patología Enfermedad degenerativa Enfermedad hereditaria Médula espinal patología Sistema nervosio central patología Sistema nervioso 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
3452901

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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