Whole exome sequencing identifies KCNQ2 mutations in Ohtahara syndrome.
Saitsu, Hirotomo; Kato, Mitsuhiro; Koide, Ayaka; Goto, Tomohide; Fujita, Takako; Nishiyama, Kiyomi; Tsurusaki, Yoshinori; Doi, Hiroshi; Miyake, Noriko; Hayasaka, Kiyoshi; Matsumoto, Naomichi; Annals of Neurology, 2012, vol. 72, issue 2, p 298, ISSN 03645134. ISBN 15318249.

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