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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Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:Ann Indian Acad Neurol
Egile Nagusiak: 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
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: Medknow Publications & Media Pvt Ltd 2016
Gaiak:
Original Article
Sarrera elektronikoa: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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