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Article

Spinocerebellar ataxia 8: variable phenotype and unique pathogenesis.

Parkinsonism & related disorders - 1 Nov 2009

Gupta Amitabh, Jankovic Joseph

Abstract excerpt

Spinocerebellar ataxia 8 (SCA8), a triplet repeat expansion disorder, is genetically distinct from the other inherited ataxias, but its unusually variable phenotype can make its diagnosis difficult. In this review we describe 3 new cases of genetically verified SCA8 to highlight the broad clinica...

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Identifiers

PMID: 19559641
DOI: 10.1016/j.parkreldis.2009.06.001

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-19559641-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

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

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