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0398 A phenotypic and genetic analysis of spinocerebellar ataxia type 2 in a Filipino family


Book ID
119466943
Publisher
Elsevier Science
Year
2005
Tongue
English
Weight
125 KB
Volume
238
Category
Article
ISSN
0022-510X

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## Abstract Spinocerebellar ataxia (SCA) types 2 and 3 are autosomal‐dominant neurodegenerative disorders caused by mutations in two different genes. We identified mutations for __SCA2__ and __SCA3__ segregating simultaneously in a single Brazilian family. The index patient had __SCA2__, whereas he

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