AB
Amina Bakhchane

Publications (3)

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

Domaines principaux

Sciences de la vie et biotechnologies2 Sciences de la santé1

Statistiques

Consultations8
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