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Article

Molecular features of the CAG repeats of spinocerebellar ataxia 6 (SCA6)

1 Aug 1997

Abstract excerpt

Spinocerebellar ataxia 6 (SCA6) is an autosomal dominant spinocerebellar degeneration caused by the expansion of the polymorphic CAG repeat in the human alpha1A voltage-dependent calcium channel subunit gene (CACNL1A4 gene). We have analyzed 60 SCA6 individuals from 39 independent SCA6 Japanese families and found that the CAG repeat length is inversely correlated with the age of onset (n = 58, r = -0.51, P <...

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PMID: 9259274
DOI: 10.1093/hmg/6.8.1283

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Molecular features of the CAG repeats of spinocerebellar ataxia 6 (SCA6)PMID 9259274Read ↗

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