AZ
Abdelali Zrhidri

Publications (3)

Clinical exome sequencing identifies two novel mutations of the SCN1A and SCN2A genes in Moroccan patients with epilepsy: a case series
Article scientifique · 2019
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

Consultations10
Téléchargements0