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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Vydáno v:Ann Indian Acad Neurol
Hlavní autoři: 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
Médium: Artigo
Jazyk:Inglês
Vydáno: Medknow Publications & Media Pvt Ltd 2016
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Original Article
On-line přístup: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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