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Clinical and molecular characteristics of a Brazilian family with spinocerebell...
Lopes-Cendes,Iscia; Steiner,Carlos E.; Silveira,Isabel; Pinto-Junior,Walter; Maciel,Jayme A.; Rouleau,Guy A.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 dentatorubropallidoluysian atrophy (DRPLA). Expansions of an unstable trinucleotide CAG repeat cause three of these disorders: SCA1, MJ...
Date: 1996
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Origin: Oasisbr