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Publications by Katsuhisa Ogata

Biallelic Mutations in MYPN , Encoding Myopalladin, Are Associated With Childhood-Onset, Slowly Progressive Nemaline Myopathy

American Journal of Human Genetics

English

Screening of Autoantibodies Associated With Necrotizing Myopathy Among Undiagnosed Chronic Myopathy

Clinical Neurology

English