GRIN2A mutations cause epilepsy-aphasia spectrum disorders

Gemma L. Carvill(University of Washington), Brigid M. Regan(Austin Health), Simone C. Yendle(University of Melbourne), Brian J. O’Roak(University of Washington), Natalia Lozovaya(Inserm), Nadine Bruneau(Institut de Neurobiologie de la Méditerranée), Nail Burnashev(Aix-Marseille Université), Adiba Khan(University of Washington), Joseph Cook(University of Washington), Eileen Geraghty(University of Washington), Lynette G. Sadleir(University of Otago), Samantha J. Turner(Austin Health), Meng‐Han Tsai(University of Melbourne), Richard Webster(Children's Hospital at Westmead), Robert Ouvrier(Children's Hospital at Westmead), John A. Damiano(Austin Health), Samuel F. Berkovic(Austin Health), Jay Shendure(University of Washington), Michael S. Hildebrand(University of Melbourne), Pierre Szepetowski(Inserm), Ingrid E. Scheffer(Royal Children's Hospital), Heather C. Mefford(University of Washington)
Nature Genetics
August 11, 2013
10.1038/ng.2727
Cited by 374Open Access
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