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Comment
. 2012 Aug;72(2):298-300.
doi: 10.1002/ana.23620.

Whole exome sequencing identifies KCNQ2 mutations in Ohtahara syndrome

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

Whole exome sequencing identifies KCNQ2 mutations in Ohtahara syndrome

Hirotomo Saitsu et al. Ann Neurol. 2012 Aug.
No abstract available

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  • KCNQ2 encephalopathy: emerging phenotype of a neonatal epileptic encephalopathy.
    Weckhuysen S, Mandelstam S, Suls A, Audenaert D, Deconinck T, Claes LR, Deprez L, Smets K, Hristova D, Yordanova I, Jordanova A, Ceulemans B, Jansen A, Hasaerts D, Roelens F, Lagae L, Yendle S, Stanley T, Heron SE, Mulley JC, Berkovic SF, Scheffer IE, de Jonghe P. Weckhuysen S, et al. Ann Neurol. 2012 Jan;71(1):15-25. doi: 10.1002/ana.22644. Ann Neurol. 2012. PMID: 22275249

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