SM
S. El Mouatassim

Publications (3)

Post-mortem diagnosis of Pompe disease by exome sequencing in a Moroccan family: a case report
Article scientifique · 2018
A novel non sense mutation in WDR62 causes autosomal recessive primary microcephaly: a case report
Article scientifique · 2018
Next Generation Sequencing identifies mutations in GNPTG gene as a cause of familial form of scleroderma-like disease
Article scientifique · 2017

Domaines principaux

Sciences de la santé2 Sciences de la vie et biotechnologies1

Statistiques

Consultations11
Téléchargements0