Next generation sequencing identifies a pathogenic mutation of WFS1 gene in a Moroccan family with Wolfram syndrome: a case report

por Sahli, Maryem, Zrhidri, Abdelali, Boualaoui, Imad, Cherkaoui Jaouad, Imane, El Kadiri, Youssef, Nouini, Yassine, Sefiani, Abdelaziz
Publicado 2023

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

Post-mortem diagnosis of Pompe disease by exome sequencing in a Moroccan family: a case report

por Adadi, Najlae, Sahli, Maryem, Egéa, Grégory, Ratbi, Ilham, Taoudi, Mohamed, Zniber, Layla, Jdioui, Wafaa, El Mouatassim, Said, Sefiani, Abdelaziz
Publicado 2018