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Article

Expansion of the Spinocerebellar ataxia type 10 (SCA10) repeat in a patient with Sioux Native American ancestry.

PloS one - 1 Jan 2013

Bushara Khalaf, Bower Matthew, Liu Jilin, McFarland Karen N, Landrian Ivette, Hutter Diane, Teive Hélio A G, Rasmussen Astrid, Mulligan Connie J, Ashizawa Tetsuo

Abstract excerpt

Spinocerebellar ataxia type 10 (SCA10), an autosomal dominant cerebellar ataxia, is caused by the expansion of the non-coding ATTCT pentanucleotide repeat in the ATAXIN 10 gene. To date, all cases of SCA10 are restricted to patients with ancestral ties to Latin American countries. Here, we report on a SCA10 patient with Sioux Native American ancestry and no reported Hispanic or Latino heritage. Neurological exam...

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Identifiers

PMID: 24278426
DOI: 10.1371/journal.pone.0081342
PMCID: PMC3835687

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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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