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Spinocerebellar ataxia type 7: Report of an Indian family

Spinocerebellar ataxia type 7 (SCA7) is a form of autosomal dominant cerebellar ataxia which is associated with pigmentary retinal degeneration. It is known for its world-wide rarity except in the Scandinavian countries. It is very rarely reported from India and the neighbouring Asian countries. The...

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Autor principal: Wali, Gurusidheshwar M.
Formato: Artigo
Lenguaje:Inglês
Publicado: Medknow Publications & Media Pvt Ltd 2013
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Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC3841638/
https://ncbi.nlm.nih.gov/pubmed/24339617
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0972-2327.120455
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