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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Detalles Bibliográficos
Autores principales: 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: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2016
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4980960/
https://www.ncbi.nlm.nih.gov/pubmed/27570389
http://dx.doi.org/10.4103/0972-2327.186823

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4980960/
https://www.ncbi.nlm.nih.gov/pubmed/27570389
http://dx.doi.org/10.4103/0972-2327.186823

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