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    Clinical phenotype features and genetic etiologies of 38 children with progressive myoclonic epilepsy

    Progressive myoclonic epilepsy (PME) is a group of neurodegenerative diseases with genetic heterogeneity and phenotypic similarities, and many cases remain unknown of the genetic causes. This study is aim to s...

    **g Zhang, Ying Yang, Xueyang Niu, Jiaoyang Chen, Wei Sun… in Acta Epileptologica (2020)

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