Association of nonsense mutation in GABRG2 with abnormal trafficking of GABAA receptors in severe epilepsy-Reference-Cited by-同舟云学术

Association of nonsense mutation in GABRG2 with abnormal trafficking of GABAA receptors in severe epilepsy

Published:2014-03 Issue:3 Volume:108 Page:420-432
ISSN:0920-1211
Container-title:Epilepsy Research
language:en
Short-container-title:Epilepsy Research

Author:

Ishii Atsushi,Kanaumi Takeshi,Sohda Miwa,Misumi Yoshio,Zhang Bo,Kakinuma Naoto,Haga Yoshiko,Watanabe Kazuyoshi,Takeda Sen,Okada Motohiro,Ueno Shinya,Kaneko Sunao,Takashima Sachio,Hirose Shinichi

Publisher

Elsevier BV

Subject

Clinical Neurology,Neurology

Reference59 articles.

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5. De novo SCN1A mutations are a major cause of severe myoclonic epilepsy of infancy;Claes;Hum. Mutat.,2003

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