Mutation in SNAP25 as a novel genetic cause of epilepsy and intellectual disability

por Rohena, Luis, Neidich, Julie, Truitt Cho, Megan, Gonzalez, Kelly DF, Tang, Sha, Devinsky, Orrin, Chung, Wendy K
Publicado 2013

A human de novo mutation in MYH10 phenocopies the loss of function mutation in mice

por Tuzovic, Lea, Yu, Lan, Zeng, Wenqi, Li, Xiang, Lu, Hong, Lu, Hsiao-Mei, Gonzalez, Kelly DF, Chung, Wendy K
Publicado 2013