GRIN2A mutations cause epilepsy-aphasia spectrum disorders

Carvill, Gemma L; Regan, Brigid M; Yendle, Simone C; O'Roak, Brian J; Lozovaya, Natalia; Bruneau, Nadine; Burnashev, Nail; Khan, Adiba; Cook, Joseph; Geraghty, Eileen; Sadleir, Lynette G; Turner, Samantha J; Tsai, Meng-Han; Webster, Richard; Ouvrier, Robert; Damiano, John A; Berkovic, Samuel F; Shendure, Jay; Hildebrand, Michael S; Szepetowski, Pierre; Scheffer, Ingrid E; Mefford, Heather C

期刊名称Nature Genetics
作者Carvill, Gemma L; Regan, Brigid M; Yendle, Simone C; O'Roak, Brian J; Lozovaya, Natalia; Bruneau, Nadine; Burnashev, Nail; Khan, Adiba; Cook, Joseph; Geraghty, Eileen; Sadleir, Lynette G; Turner, Samantha J; Tsai, Meng-Han; Webster, Richard; Ouvrier, Robert; Damiano, John A; Berkovic, Samuel F; Shendure, Jay; Hildebrand, Michael S; Szepetowski, Pierre; Scheffer, Ingrid E; Mefford, Heather C
卷第45卷
期第9期
印刷ISSN1061-4036
电子ISSN1546-1718
文件大小547.61KB
发表时间2013-8-11
DOI10.1038/ng.2727
页码1073-1076

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GRIN2A mutations cause epilepsy-aphasia spectrum disorders