YK
Yamna Kriouile

Publications (3)

First Characterization of Congenital Myasthenic Syndrome Type 5 in North Africa
Article scientifique · 2021
Identification of a novel LAMA2 c.2217G > A, p.(Trp739*) mutation in a Moroccan patient with congenital muscular dystrophy: a case report
Article scientifique · 2021
Management of X-linked adrenoleukodystrophy in Morocco: actual situation
Article scientifique · 2017

Domaines principaux

Sciences de la vie et biotechnologies2 Sciences de la santé1

Statistiques

Consultations9
Téléchargements0