Ghita Amalou

Clinical and genetic spectrums of 413 North African families with inherited retinal dystrophies and optic neuropathies

Majida Charif, G. Lenaers, H. Charoute, 2022, Orphanet Journal of Rare Diseases.

A homozygous nonsense HECW2 variant is associated with neurodevelopmental delay and intellectual disability.

Majida Charif, G. Lenaers, H. Charoute, 2022, European journal of medical genetics.

First characterization of LTBP3 variants in two Moroccan families with hypoplastic amelogenesis imperfecta.

Majida Charif, G. Lenaers, H. Charoute, 2022, Archives of oral biology.

Genetic heterogeneity in GJB2, COL4A3, ATP6V1B1 and EDNRB variants detected among hearing impaired families in Morocco

C. Petit, H. Charoute, H. Rouba, 2021, Molecular Biology Reports.

Computational Analysis of nsSNPs of ADA Gene in Severe Combined Immunodeficiency Using Molecular Modeling and Dynamics Simulation

H. Rouba, A. Barakat, Zouhair Elkarhat, 2019, Journal of immunology research.