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Unexplained early onset epileptic encephalopathy: Exome screening and phenotype expansion.

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第一作者: Nicholas M,Allen
第一单位: Department of Paediatric Neurology and Clinical Neurophysiology, Children's University Hospital, Dublin, Ireland.
作者单位: Department of Paediatric Neurology and Clinical Neurophysiology, Children's University Hospital, Dublin, Ireland. [1] Department of Paediatric Neurology and Clinical Neurophysiology, Children's University Hospital, Dublin, Ireland.;Academic Centre on Rare Diseases, School of Medicine and Medical Science, University College Dublin, Dublin, Ireland. [2] Laboratory of Clinical Genomics, Faculty of Medicine of Universidade Federal de Minas Gerais, Belo Horizonte, Brazil. [3] Academic Centre on Rare Diseases, School of Medicine and Medical Science, University College Dublin, Dublin, Ireland.;The National Children's Research Centre, Our Lady's Children's Hospital Crumlin, Dublin 12, Ireland. [4] Academic Centre on Rare Diseases, School of Medicine and Medical Science, University College Dublin, Dublin, Ireland. [5]
DOI 10.1111/epi.13250
PMID 26648591
发布时间 2022-04-08
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Epilepsia

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