Genetic Screening for Spinocerebellar Ataxia Genes in a Japanese Single-Hospital Cohort

Genetic Screening for Spinocerebellar Ataxia Genes in a Japanese Single-Hospital Cohort

Objective Diagnosis of sporadic cerebellar ataxia is a challenge for neurologists. A wide range of potential causes exist, including chronic alcohol use, multiple system atrophy of cerebellar type (MSA-C), and sporadic late cortical cerebellar atrophy. Recently, an autosomal-dominant spinocerebellar...

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Bibliographic Details
Main Authors: Ryuji Sakakibara, Fuyuki Tateno, Masahiko Kishi, Yohei Tsuyusaki, Yosuke Aiba, Hitoshi Terada, Tsutomu Inaoka, Setsu Sawai, Satoshi Kuwabara, Fumio Nomura
Format: Article
Language:English
Published: Korean Movement Disorders Society 2017-09-01
Series:Journal of Movement Disorders
Subjects:
Sporadic
cerebellar ataxia
spinocerebellar ataxia type 6
heredity
Online Access:http://www.e-jmd.org/upload/jmd-17011.pdf

Internet

http://www.e-jmd.org/upload/jmd-17011.pdf

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