Whole exome sequencing identifies KCNQ2 mutations in Ohtahara syndrome-Reference-Cited by-同舟云学术

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Whole exome sequencing identifies KCNQ2 mutations in Ohtahara syndrome

Published:2012-08 Issue:2 Volume:72 Page:298-300
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol.

Author:

Saitsu Hirotomo,Kato Mitsuhiro,Koide Ayaka,Goto Tomohide,Fujita Takako,Nishiyama Kiyomi,Tsurusaki Yoshinori,Doi Hiroshi,Miyake Noriko,Hayasaka Kiyoshi,Matsumoto Naomichi

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ana.23620/fullpdf

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