FL
Fatima Zahra Laarabi

Publications (5)

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
Homozygous frameshift mutations in FAT1 cause a syndrome characterized by colobomatous-microphthalmia, ptosis, nephropathy and syndactyly
Article scientifique · 2019
A novel single variant in the MEFV gene causing Mediterranean fever and Behçet’s disease: a case report
Article scientifique · 2018
A novel frameshift mutation in the XPC gene in a Moroccan patient: a case report
Article scientifique · 2017
High frequency of the recurrent c.1310_1313delAAGA BRCA2 mutation in the North-East of Morocco and implication for hereditary breast–ovarian cancer prevention and control
Article scientifique · 2017

Domaines principaux

Sciences de la vie et biotechnologies5

Statistiques

Consultations20
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