Characterisation of mutations of the phosphoinositide-3-kinase regulatory subunit, PIK3R2, in perisylvian polymicrogyria: a next-generation sequencing study-Reference-Cited by-同舟云学术

Characterisation of mutations of the phosphoinositide-3-kinase regulatory subunit, PIK3R2, in perisylvian polymicrogyria: a next-generation sequencing study

Published:2015-12 Issue:12 Volume:14 Page:1182-1195
ISSN:1474-4422
Container-title:The Lancet Neurology
language:en
Short-container-title:The Lancet Neurology

Author:

Mirzaa Ghayda M,Conti Valerio,Timms Andrew E,Smyser Christopher D,Ahmed Sarah,Carter Melissa,Barnett Sarah,Hufnagel Robert B,Goldstein Amy,Narumi-Kishimoto Yoko,Olds Carissa,Collins Sarah,Johnston Kathreen,Deleuze Jean-François,Nitschké Patrick,Friend Kathryn,Harris Catharine,Goetsch Allison,Martin Beth,Boyle Evan August,Parrini Elena,Mei Davide,Tattini Lorenzo,Slavotinek Anne,Blair Ed,Barnett Christopher,Shendure Jay,Chelly Jamel,Dobyns William B,Guerrini Renzo

Funder

US National Institutes of Health under NINDS grants

EU Seventh Framework Programme

Publisher

Elsevier BV

Subject

Clinical Neurology

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