Clinical exome sequencing identifies two novel mutations of the SCN1A and SCN2A genes in Moroccan patients with epilepsy: a case series

por Sahli, Maryem, Zrhidri, Abdelali, Elaloui, Siham Chafai, Smaili, Wiam, Lyahyai, Jaber, Oudghiri, Fatima Zohra, Sefiani, Abdelaziz
Publicado 2019