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Article

Spinocerebellar ataxia type 10 - A review.

Parkinsonism & related disorders - 1 Nov 2011

Teive Hélio A G, Munhoz Renato P, Arruda Walter O, Raskin Salmo, Werneck Lineu César, Ashizawa Tetsuo

Abstract excerpt

Spinocerebellar ataxia type 10 (SCA10) is an autosomal dominant inherited ataxia caused by an expanded ATTCT pentanucleotide repeat in intron 9 of the ATXN10 gene, on chromosome 22q13.3. SCA10 represents a rare form of SCA, until now only described in Latin America, particularly in Mexico, Brazil, Argentina and Venezuela. In Mexico and Brazil SCA10 represents the second most common type of autosomal dominant...

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Identifiers

PMID: 21531163
DOI: 10.1016/j.parkreldis.2011.04.001

Genes

ATXN10

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

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