Spinocerebellar ataxia type 6 in eastern India: Some new observations

INTRODUCTION: Spinocerebellar ataxias (SCAs) are hereditary, autosomal dominant progressive neurodegenerative disorders showing clinical and genetic heterogeneity. They are usually manifested clinically in the third to fifth decade of life although there is a wide variability in the age of onset. Mo...

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Detalhes bibliográficos
Publicado no:Ann Indian Acad Neurol
Main Authors: Bhattacharyya, Kalyan B, Pulai, Debabrata, Guin, Deb Shankar, Ganguly, Goutam, Joardar, Anindita, Roy, Sarnava, Rai, Saurabh, Biswas, Atanu, Pandit, Alok, Roy, Arijit, Senapati, Asit Kumar
Formato: Artigo
Idioma:Inglês
Publicado em: Medknow Publications & Media Pvt Ltd 2016
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Original Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4980960/
https://ncbi.nlm.nih.gov/pubmed/27570389
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0972-2327.186823
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