Spinocerebellar ataxia type 10 (SCA10): Mutation analysis and common haplotype based inference suggest its rarity in Indian population

Spinocerebellar ataxia type 10 (SCA10) is a rare autosomal dominant cerebellar ataxia caused by nucleotide ATTCT expansion in ATXN10 gene. SCA10 has been reported in patients of cerebellar ataxia from Amerindian/Latin America and in East Asian ancestry. A common founder has been ascribed to the orig...

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Detalles Bibliográficos
Autores principales: Goel, Divya, Suroliya, Varun, Shamim, Uzma, Mathur, Aradhna, Faruq, Mohammed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6849144/
https://www.ncbi.nlm.nih.gov/pubmed/31737797
http://dx.doi.org/10.1016/j.ensci.2019.100211

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6849144/
https://www.ncbi.nlm.nih.gov/pubmed/31737797
http://dx.doi.org/10.1016/j.ensci.2019.100211

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