Journal
CEREBELLUM
Volume 4, Issue 1, Pages 31-36Publisher
TAYLOR & FRANCIS LTD
DOI: 10.1080/14734220410026248
Keywords
spinocerebellar ataxia type 3; ataxin-3; heat shock protein 27; cell death
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Spinocerebellar ataxia type 3 (SCA3) is an autosomal dominant spinocerebellar degeneration characterized by a wide range of clinical manifestations. In this review, we discuss the role(s) that heat shock protein 27 (HSP27) may play in the cell death process of spinocerebellar ataxia type 3.
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