Novel <em>PRKCG</em> mutations in Japanese autosomal dominant spinocerebellar ataxia

Yui Tada Tada

[1P-229] Novel PRKCG mutations in Japanese autosomal dominant spinocerebellar ataxia

*Yui Tada Tada¹, Kodai Kume¹, Soma Noguchi², Ryosuke Ohsawa¹, Norio Sakai², Hideshi Kawakami¹ (1. RIRBM, Hiroshima Univ, Hiroshimaa, Japan, 2. Grad Sch Biomed & Health Sci, Hiroshima Univ, Hiroshimaa, Japan)

Keywords:Spinocerebellar ataxia, PRKCG

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PW: Neuro2022

Presentation information

[1P] F. Disorders of the Nervous System 2

[1P-229] Novel PRKCG mutations in Japanese autosomal dominant spinocerebellar ataxia

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