Whole exome sequencing identifies KCNQ2 mutations in Ohtahara syndrome.
Saitsu H; Kato M; Koide A; Goto T; Fujita T; Nishiyama K; Tsurusaki Y; Doi H; Miyake N; Hayasaka K; Matsumoto N; Annals Of Neurology, 2012, vol. 72, issue 2, p 298, ISSN 15318249. ISBN 15318249.

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