Mutations of Neuronal Voltage-gated Na+ Channel alpha1 Subunit Gene SCN1A in Core Severe Myoclonic Epilepsy in Infancy (SMEI) and in Borderline SMEI (SMEB)-Reference-Cited by-同舟云学术

Mutations of Neuronal Voltage-gated Na+ Channel alpha1 Subunit Gene SCN1A in Core Severe Myoclonic Epilepsy in Infancy (SMEI) and in Borderline SMEI (SMEB)

Published:2004-02 Issue:2 Volume:45 Page:140-148
ISSN:0013-9580
Container-title:Epilepsia
language:en
Short-container-title:Epilepsia

Author:

Fukuma Goryu,Oguni Hirokazu,Shirasaka Yukiyoshi,Watanabe Kazuyoshi,Miyajima Tasuku,Yasumoto Sawa,Ohfu Masaharu,Inoue Takahito,Watanachai Aruchalean,Kira Ryutaro,Matsuo Muneaki,Muranaka Hideki,Sofue Fumiko,Zhang Bo,Kaneko Sunao,Mitsudome Akihisa,Hirose Shinichi

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.0013-9580.2004.15103.x/fullpdf

Reference22 articles.

1. Genetics of epilepsy: current status and perspectives

2. Severe myoclonic epilepsy in infants – a review based on the Tokyo Women's Medical University series of 84 cases

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