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Two definite cases of sudden unexpected death in epilepsy in a family with a DEPDC5 mutation.

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第一作者： Fábio A,Nascimento

第一单位： Division of Neurology (F.A.N., F.B., D.M.A.), Epilepsy Genetics Program, Krembil Neuroscience Centre, Toronto Western Hospital, University of Toronto, Ontario, Canada; CHUM Research Center (P.C.), University of Montreal, Quebec, Canada; and Division of Neurology (B.A.M., D.M.A.), Program in Genetics and Genome Biology, The Hospital for Sick Children, University of Toronto, Ontario, Canada.

作者： Fábio A,Nascimento ^[1] ; Felippe,Borlot ^[1] ; Patrick,Cossette ^[1] ; Berge A,Minassian ^[1] ; Danielle M,Andrade ^[1]

作者单位： Division of Neurology (F.A.N., F.B., D.M.A.), Epilepsy Genetics Program, Krembil Neuroscience Centre, Toronto Western Hospital, University of Toronto, Ontario, Canada; CHUM Research Center (P.C.), University of Montreal, Quebec, Canada; and Division of Neurology (B.A.M., D.M.A.), Program in Genetics and Genome Biology, The Hospital for Sick Children, University of Toronto, Ontario, Canada. ^[1]

DOI 10.1212/NXG.0000000000000028

PMID 27066565

发布时间 2020-10-01

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Two definite cases of sudden unexpected death in epilepsy in a family with a DEPDC5 mutation.

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