WS
Wiam Smaili

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 frameshift mutation in the XPC gene in a Moroccan patient: a case report
Article scientifique · 2017
A novel TRPS1 mutation in a Moroccan family with Tricho-rhino-phalangeal syndrome type III: case report
Article scientifique · 2017

Domaines principaux

Sciences de la vie et biotechnologies2 Sciences de la santé1

Statistiques

Consultations9
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