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A homozygous MPZL2 deletion is associated with non syndromic hearing loss in a moroccan family

Ghita Amalou , Crystel Bonnet , Zied Riahi , Aymane Bouzidi , Soukaina Elrharchi , et al.
International Journal of Pediatric Otorhinolaryngology, 2021, 140, pp.110481. ⟨10.1016/j.ijporl.2020.110481⟩
Journal articles pasteur-03215242v1

Characterizing subcutaneous cortical auditory evoked potentials in mice

Olivier Postal , Warren Bakay , Typhaine Dupont , Alexa Buck , Christine Petit , et al.
Hearing Research, 2022, 422, pp.108566. ⟨10.1016/j.heares.2022.108566⟩
Journal articles hal-03852440v1

Novel Mutation in AIFM1 Gene Associated with X-Linked Deafness in a Moroccan Family

Soukaina Elrharchi , Zied Riahi , Sara Salime , Hicham Charoute , Lamiae Elkhattabi , et al.
Human Heredity, 2021, 85 (1), pp.35-39. ⟨10.1159/000512712⟩
Journal articles pasteur-03219602v1

Identification a novel pathogenic LRTOMT mutation in Mauritanian families with nonsyndromic deafness

Malak Salame , Crystel Bonnet , Ely Cheikh Mohamed Moctar , Selma Mohamed Brahim , Abdallahi Dedy , et al.
European Archives of Oto-Rhino-Laryngology, 2023, ⟨10.1007/s00405-023-07907-z⟩
Journal articles pasteur-04053511v1

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

Imane Aitraise , Ghita Amalou , Amale Bousfiha , Hicham Charoute , Hassan Rouba , et al.
Molecular Biology Reports, 2022, 49 (5), pp.3949-3954. ⟨10.1007/s11033-022-07245-z⟩
Journal articles pasteur-03985530v1