De Novo Mutations inGNAO1, Encoding a G╬▒oSubunit of Heterotrimeric G Proteins, Cause Epileptic Encephalopathy


Kazuyuki Nakamura,Hirofumi Kodera,Tenpei Akita,Masaaki Shiina,Mitsuhiro Kato,Hideki Hoshino,Hiroshi Terashima,Hitoshi Osaka,Shinichi Nakamura,Jun Tohyama,Tatsuro Kumada,Tomonori Furukawa,Satomi Iwata,Takashi Shiihara,Masaya Kubota,Satoko Miyatake, et al.


The American Journal of Human Genetics




5 September 2013

Copyright © 2013, Elsevier

 User ID  
 Enable Auto Login
Forgot Password/User ID?
If you're a copyright.com user, you can login to RightsLink using your copyright.com credentials.
Already a RightsLink user or want to learn more?

Welcome to RightsLink

Elsevier has partnered with Copyright Clearance Center's RightsLink service to offer a variety of options for reusing Elsevier content. Select the "I would like to ..." drop-down menu to view the many reuse options available to you.

I would like to...


To request permission for a type of use not listed, please contact Elsevier Global Rights Department.

Are you the author of this Elsevier journal article?


Copyright © 2014 Copyright Clearance Center, Inc. All Rights Reserved. Privacy statement.
Comments? We would like to hear from you. E-mail us at customercare@copyright.com