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Publications by Yukiko K. Hayashi

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

American Journal of Human Genetics
Genetics
2017English

Pathology of Frontotemporal Dementia With Limb Girdle Muscular Dystrophy Caused by a DNAJB6 Mutation

Clinical Neurology and Neurosurgery
MedicineSurgeryNeurology
2014English

A Novel POMT2 Mutation Causes Mild Congenital Muscular Dystrophy With Normal Brain MRI

Brain and Development
Child HealthDevelopmental NeurosciencePerinatologyNeurologyMedicinePediatrics
2009English

Limb-Girdle Muscular Dystrophy Due to Emerin Gene Mutations

Archives of Neurology
2007English

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