Clinical and molecular characteristics of a Brazilian family with spinocerebellar ataxia type 1

The spinocerebellar ataxias (SCAs) are a clinically and genetically heterogeneous group of late onset neurodegenerative disorders. To date, seven different genes causing autosomal dominant SCA have been mapped: SCA1, SCA2, Machado-Joseph disease (MJD)/SCA3, SCA4, SCA5, SCA7 and dentatorubropallidolu...

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Detalhes bibliográficos
Autor principal: Lopes-Cendes,Iscia (author)
Outros Autores: Steiner,Carlos E. (author), Silveira,Isabel (author), Pinto-Junior,Walter (author), Maciel,Jayme A. (author), Rouleau,Guy A. (author)
Formato: article
Idioma:eng
Publicado em: 1996
Assuntos:
neurodegenerative disease
spinocerebellar ataxia
trinucleotide expansion
Texto completo:http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0004-282X1996000300009
País:Brasil
Oai:oai:scielo:S0004-282X1996000300009

Texto Completo

http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0004-282X1996000300009

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