ITPR1 gene p.Val1553Met mutation in Russian family with mild Spinocerebellar ataxia

BACKGROUND: Spinocerebellar ataxias (SСAs) are a highly heterogeneous group of inherited neurological disorders. The symptoms of ataxia vary in individual patients and even within the same SCA subtype. A study of a four-generation family with autosomal dominant (AD) non-progressive SCA with mild sym...

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Bibliographic Details
Published in:	Cerebellum Ataxias
Main Authors:	Shadrina, M. I., Shulskaya, M. V., Klyushnikov, S. A., Nikopensius, T., Nelis, M., Kivistik, P. A., Komar, A. A., Limborska, S. A., Illarioshkin, S. N., Slominsky, P. A.
Format:	Artigo
Language:	Inglês
Published:	BioMed Central 2016
Subjects:	Research
Online Access:	https://ncbi.nlm.nih.gov/pmc/articles/PMC4712497/ https://ncbi.nlm.nih.gov/pubmed/26770814 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s40673-016-0040-8
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ITPR1 gene p.Val1553Met mutation in Russian family with mild Spinocerebellar ataxia

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