Referenced in: none

Automatically associated channels: Kv7.2

Title: Whole exome sequencing identifies KCNQ2 mutations in Ohtahara syndrome.

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

Journal, date & volume: Ann. Neurol., 2012 Aug , 72, 298-300

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/22926866

Abstract