Expansion of the Spinocerebellar Ataxia Type 10

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...

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Bibliographic Details

Published in:	PloS one Vol. 8; no. 11; p. e81342
Main Authors:	Bushara, Khalaf, Bower, Matthew, Liu, Jilin, McFarland, Karen N, Landrian, Ivette, Hutter, Diane, Teive, Hélio A. G, Rasmussen, Astrid, Mulligan, Connie J, Ashizawa, Tetsuo
Format:	Journal Article
Language:	English
Published:	Public Library of Science 20-11-2013
Subjects:	Analysis Native Americans Natural language processing Single nucleotide polymorphisms Spinocerebellar ataxias
Online Access:	Get full text
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