AB
Abdelhamid Barakat

Publications (4)

Genetic investigation of XPA gene: high frequency of the c.682C>T mutation in Moroccan XP patients with moderate clinical profile
Article scientifique · 2017
Novel compound heterozygous MYO7A mutations in Moroccan families with autosomal recessive non-syndromic hearing loss
Article scientifique · 2017
A novel PEX1 mutation in a Moroccan family with Zellweger spectrum disorders
Article scientifique · 2017
Loss of function of Ywhah in mice induces deafness and cochlear outer hair cells' degeneration
Article scientifique · 2016

Domaines principaux

Sciences de la vie et biotechnologies3 Sciences de la santé1

Statistiques

Consultations10
Téléchargements0