Novel KCNQ3 Mutation in a Large Family with Benign Familial Neonatal Epilepsy: A Rare Cause of Neonatal Seizures

Publisher： Karger

E-ISSN： 1661-8777|7|4|189-196

ISSN： 1661-8769

Source： Molecular Syndromology, Vol.7, Iss.4, 2016-07, pp. : 189-196

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