Spinocerebellar ataxia 7 (SCA7) in Indian population: predilection of ATXN7-CAG expansion mutation in an ethnic population

BACKGROUND & OBJECTIVES: Spinocerebellar ataxia 7 (SCA7) is a rare form of neurodegenerative disorder with the clinical manifestation of cerebellar ataxia and retinal degeneration. In this study we describe the clinico-genetic characteristics of nine SCA7 families of Indian origin and cross comp...

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Vydáno v:Indian J Med Res
Hlavní autoři: Faruq, Mohammed, Srivastava, Achal Kumar, Singh, Suman, Gupta, Rohit, Dada, Tanuj, Garg, Ajay, Behari, Madhuri, Mukerji, Mitali
Médium: Artigo
Jazyk:Inglês
Vydáno: Medknow Publications & Media Pvt Ltd 2015
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Original Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC4418155/
https://ncbi.nlm.nih.gov/pubmed/25900954
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