A de novo heterozygous mutation in KCNC2 gene implicated in severe developmental and epileptic encephalopathy

Bibliographic Details
Title: A de novo heterozygous mutation in KCNC2 gene implicated in severe developmental and epileptic encephalopathy
Authors: Vetri, Luigi, Calì, Francesco, Vinci, Mirella, Amato, Carmelo, Roccella, Michele, Granata, Tiziana, Freri, Elena, Solazzi, Roberta, Romano, Valentino, Elia, Maurizio
Source: In European Journal of Medical Genetics April 2020 63(4)
Database: ScienceDirect
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ISSN:17697212
DOI:10.1016/j.ejmg.2020.103848
Published in:European Journal of Medical Genetics
Language:English