Spinocerebellar ataxia type 1 and Machado-Joseph disease: incidence of CAG expansions among adult-onset ataxia patients from 311 families with dominant, recessive, or sporadic ataxia.

The ataxias are a complex group of diseases with both environmental and genetic causes. Among the autosomal dominant forms of ataxia the genes for two, spinocerebellar ataxia type 1 (SCA1) and Machado-Joseph disease (MJD), have been isolated. In both of these disorders the molecular basis of disease...

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Detalhes bibliográficos
Main Authors: Ranum, L P, Lundgren, J K, Schut, L J, Ahrens, M J, Perlman, S, Aita, J, Bird, T D, Gomez, C, Orr, H T
Formato: Artigo
Idioma:Inglês
Publicado em: 1995
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1801263/
https://ncbi.nlm.nih.gov/pubmed/7668288
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