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Transgenic Models of Spinocerebellar Ataxia Type 10: Modeling a Repeat Expansion Disorder

Spinocerebellar ataxia type 10 (SCA10) is an autosomal dominant neurodegenerative disease with a spectrum of phenotypes. SCA10 is caused by a pentanucleotide repeat expansion of the ATTCT motif within intron 9 of ATAXIN 10 (ATXN10). Patients present with cerebellar ataxia; however, a subset also dev...

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Hlavní autoři: McFarland, Karen N., Ashizawa, Tetsuo
Médium: Artigo
Jazyk:Inglês
Vydáno: MDPI 2012
Témata:
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC3899997/
https://ncbi.nlm.nih.gov/pubmed/24533179
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/genes3030481
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