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Article

The hereditary spinocerebellar ataxias in Japan.

Cytogenetic and genome research - 1 Jan 2003

Sasaki H, Yabe I, Tashiro K

Abstract excerpt

In Japan, multiple system atrophy (MSA) accounts for 40% of all spinocerebellar ataxias (SCAs) and hereditary disorders account for 30%. Among the latter, autosomal dominant disorders are common and recessive ataxias are rare. Although the frequency of SCA genotypes differs between geographic reg...

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PMID: 14526181
DOI: 10.1159/000072855

Genes

GAA

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-14526181-2026-09-02.1. Manifest publication-graph-cohort-2026-09-02.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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