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Article

Autosomal dominant cerebellar ataxia: SCA2 is the most frequent mutation in eastern India.

Journal of neurology, neurosurgery, and psychiatry - 1 Mar 2004

Sinha K K, Worth P F, Jha D K, Sinha S, Stinton V J, Davis M B, Wood N W, Sweeney M G, Bhatia K P

Abstract excerpt

OBJECTIVE: Spinocerebellar ataxia type 2 (SCA2) has been reported as the commonest dominant hereditary ataxia in India. However, India is an ethnically and religiously diverse population. Previous studies have not clearly indicated exact ethnic and religious origins, and must therefore be interpreted with caution. The purpose of this study was to determine the prevalence of different SCA mutations in a relatively...

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Identifiers

PMID: 14966163
DOI: 10.1136/jnnp.2002.004895
PMCID: PMC1738947

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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