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A de novo heterozygous mutation in KCNC2 gene implicated in severe developmental and epileptic encephalopathy
Luigi Vetri, Francesco Calì, Mirella Vinci, Carmelo Amato, Michele Roccella, Tiziana Granata, Elena Freri, Roberta Solazzi, Valentino Romano, Maurizio Elia
Research output: Contribution to journal › Article › peer-review