HR
Hassan Rouba

Publications (2)

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

Domaines principaux

Sciences de la santé1 Sciences de la vie et biotechnologies1

Statistiques

Consultations5
Téléchargements0