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A POLG2 Homozygous Mutation in an Autosomal Recessive Epilepsy Family Without Ophthalmoplegia
Article in En | WPRIM | ID: wpr-764323
Responsible library: WPRO
ABSTRACT
No abstract available.
Subject(s)
Full text: 1 Index: WPRIM Main subject: Ophthalmoplegia / Epilepsy Limits: Humans Language: En Journal: Journal of Clinical Neurology Year: 2019 Type: Article
Full text: 1 Index: WPRIM Main subject: Ophthalmoplegia / Epilepsy Limits: Humans Language: En Journal: Journal of Clinical Neurology Year: 2019 Type: Article