Microchromosomal deletions involvingSCN1Aand adjacent genes in severe myoclonic epilepsy in infancy-Reference-Cited by-同舟云学术

Microchromosomal deletions involvingSCN1Aand adjacent genes in severe myoclonic epilepsy in infancy

Published:2008-09 Issue:9 Volume:49 Page:1528-1534
ISSN:0013-9580
Container-title:Epilepsia
language:en
Short-container-title:

Author:

Wang Ji-wen,Kurahashi Hirokazu,Ishii Atsushi,Kojima Toshio,Ohfu Masaharu,Inoue Takahito,Ogawa Atsushi,Yasumoto Sawa,Oguni Hirokazu,Kure Shigeo,Fujii Tatsuya,Ito Masatoshi,Okuno Takehiko,Shirasaka Yukiyoshi,Natsume Jun,Hasegawa Aki,Konagaya Akihiko,Kaneko Sunao,Hirose Shinichi

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1528-1167.2008.01609.x/fullpdf

Reference37 articles.

1. Clinical correlations of mutations in the SCN1A gene: from febrile seizures to severe myoclonic epilepsy in infancy;Ceulemans;Pediatr Neurol,2004

2. De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancy;Claes;Am J Hum Genet,2001

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

4. An SCN9A channelopathy causes congenital inability to experience pain;Cox;Nature,2006

5. Electrophysiological properties of mutant Nav1.7 sodium channels in a painful inherited neuropathy;Cummins;J Neurosci,2004

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