Title : A knockin mouse model of spinocerebellar ataxia type 3 exhibits prominent aggregate pathology and aberrant splicing of the disease gene transcript.

Pub. Date : 2015 Mar 1

PMID : 25320121






1 Functional Relationships(s)
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1 Polyglutamine diseases, including spinocerebellar ataxia type 3 (SCA3), are caused by CAG repeat expansions that encode abnormally long glutamine repeats in the respective disease proteins. polyglutamine ataxin 3 Mus musculus