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Progressive Myoclonic Epilepsy Type 8 Due to CERS1 Deficiency: A Novel Mutation with Prominent Ataxia
Author(s) -
Godeiro Junior Clécio de Oliveira,
Vale Thiago Cardoso,
Afonso Cintia Oliveira de Melo,
Kok Fernando,
Pedroso José Luiz,
Barsottini Orlando G.
Publication year - 2018
Publication title -
movement disorders clinical practice
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.754
H-Index - 18
ISSN - 2330-1619
DOI - 10.1002/mdc3.12610
Subject(s) - progressive myoclonus epilepsy , epilepsy , ataxia , myoclonic epilepsy , medicine , mutation , myoclonus , neuroscience , psychology , genetics , biology , gene
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