Ilham Ratbi

The Moroccan human mutation database

Abdelaziz Sefiani, A. Sefiani, I. Ratbi, 2008, Indian journal of human genetics.

A mutation in CALM1 encoding calmodulin in familial idiopathic ventricular fibrillation in childhood and adolescence.

Marielle Alders, Abdelaziz Sefiani, A. Wilde, 2014, Journal of the American College of Cardiology.

GNB5 Mutations Cause an Autosomal-Recessive Multisystem Syndrome with Sinus Bradycardia and Cognitive Disability.

Nicolas Guex, Arthur A M Wilde, Alexandre Reymond, 2016, American journal of human genetics.

First application of next-generation sequencing in Moroccan breast/ovarian cancer families and report of a novel frameshift mutation of the BRCA1 gene.

Abdelaziz Sefiani, S. Elalaoui, A. Sefiani, 2016, Oncology letters.

GNB5 Mutations Cause an Autosomal-Recessive Multisystem Syndrome with Sinus Bradycardia and Cognitive Disability.

Nicolas Guex, Arthur A M Wilde, Alexandre Reymond, 2016, American journal of human genetics.