Spinocerebellar ataxia type 6 in eastern India: Some new observations

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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Bibliographic Details
Main Authors: Kalyan B Bhattacharyya, Debabrata Pulai, Deb Shankar Guin, Goutam Ganguly, Anindita Joardar, Sarnava Roy, Saurabh Rai, Atanu Biswas, Alok Pandit, Arijit Roy, Asit Kumar Senapati
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2016-01-01
Series:Annals of Indian Academy of Neurology
Subjects:
Eastern India
SCA6
Spinocerebellar ataxia
Online Access:http://www.annalsofian.org/article.asp?issn=0972-2327;year=2016;volume=19;issue=3;spage=360;epage=366;aulast=Bhattacharyya

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http://www.annalsofian.org/article.asp?issn=0972-2327;year=2016;volume=19;issue=3;spage=360;epage=366;aulast=Bhattacharyya

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