AB
Amale Bousfiha

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

Consultations7
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