Recessive TBC1D24 Mutations Are Frequent in Moroccan Non-Syndromic Hearing Loss Pedigrees

por Bakhchane, Amina, Charif, Majida, Salime, Sara, Boulouiz, Redouane, Nahili, Halima, Roky, Rachida, Lenaers, Guy, Barakat, Abdelhamid
Publicado 2015

Novel compound heterozygous MYO7A mutations in Moroccan families with autosomal recessive non-syndromic hearing loss

por Bakhchane, Amina, Charif, Majida, Bousfiha, Amale, Boulouiz, Redouane, Nahili, Halima, Rouba, Hassan, Charoute, Hicham, Lenaers, Guy, Barakat, Abdelhamid
Publicado 2017

Prediction of the Impact of Deleterious Nonsynonymous Single Nucleotide Polymorphisms on the Human RRM2B Gene: A Molecular Modeling Study

por Ait El Cadi, Chaimaa, Krami, Al Mehdi, Charoute, Hicham, Elkarhat, Zouhair, Sifeddine, Najat, Lakhiari, Hamid, Rouba, Hassan, Barakat, Abdelhamid, Nahili, Halima
Publicado 2020

Genetic and molecular analysis of the CLDN14 gene in Moroccan family with non-syndromic hearing loss

por Charif, Majida, Boulouiz, Redouane, Bakhechane, Amina, Benrahma, Houda, Nahili, Halima, Eloualid, Abdelmajid, Rouba, Hassan, Kandil, Mostafa, Abidi, Omar, Lenaers, Guy, Barakat, Abdelhamid
Publicado 2013