Expansion of the Spinocerebellar Ataxia Type 10 (SCA10) Repeat in a Patient with Sioux Native American Ancestry

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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Detaylı Bibliyografya
Asıl Yazarlar: Bushara, Khalaf, Bower, Matthew, Liu, Jilin, McFarland, Karen N., Landrian, Ivette, Hutter, Diane, Teive, Hélio A. G., Rasmussen, Astrid, Mulligan, Connie J., Ashizawa, Tetsuo
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Public Library of Science 2013
Konular:
Research Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC3835687/
https://ncbi.nlm.nih.gov/pubmed/24278426
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0081342
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