AB
Abdelhamid Barakat

Publications (10)

Clinical and Genetic Spectrum of MEFV Variants in Moroccan Patients with Familial Mediterranean Fever
Article scientifique · 2026
Unlocking the African bioeconomy and strengthening biodiversity conservation through genomics and bioinformatics
Article scientifique · 2025
Clinical and genetic spectrums of 413 North African families with inherited retinal dystrophies and optic neuropathies
Article scientifique · 2022
Association of HNF1A gene variants and haplotypes with metabolic syndrome: a case–control study in the Tunisian population and a meta-analysis
Article scientifique · 2022
Genetic Heterogeneity in GJB2, COL4A3, ATP6V1B1 and EDNRB Variants Detected Among Hearing Impaired Families in Morocco
Article scientifique · 2021
First Characterization of Congenital Myasthenic Syndrome Type 5 in North Africa
Article scientifique · 2021
Genetic investigation of XPA gene: high frequency of the c.682C>T mutation in Moroccan XP patients with moderate clinical profile
Article scientifique · 2017
Novel compound heterozygous MYO7A mutations in Moroccan families with autosomal recessive non-syndromic hearing loss
Article scientifique · 2017
A novel PEX1 mutation in a Moroccan family with Zellweger spectrum disorders
Article scientifique · 2017
Loss of function of Ywhah in mice induces deafness and cochlear outer hair cells' degeneration
Article scientifique · 2016

Domaines principaux

Sciences de la vie et biotechnologies6 Sciences de la santé4

Statistiques

Consultations27
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