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 spinocerebella...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:J Mov Disord
Prif Awduron: Sakakibara, Ryuji, Tateno, Fuyuki, Kishi, Masahiko, Tsuyusaki, Yohei, Aiba, Yosuke, Terada, Hitoshi, Inaoka, Tsutomu, Sawai, Setsu, Kuwabara, Satoshi, Nomura, Fumio
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: The Korean Movement Disorder Society 2017
Pynciau:
Original Article
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC5615168/
https://ncbi.nlm.nih.gov/pubmed/28782341
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.14802/jmd.17011
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