Sara Salime

A novel mutation of AFG3L2 might cause dominant optic atrophy in patients with mild intellectual disability

Majida Charif, Agathe Roubertie, Sara Salime et al. · Frontiers in Genetics · 2015 · 45 citations · Full text

Update of the spectrum of GJB2 gene mutations in 152 Moroccan families with autosomal recessive nonsyndromic hearing loss

Amina Bakhchane, Amale Bousfiha, Hicham Charoute et al. · European Journal of Medical Genetics · 2016 · 28 citations

Developmental Biology, Mendelian Disorder, Genetic Disorder +11

Recessive TBC1D24 Mutations Are Frequent in Moroccan Non-Syndromic Hearing Loss Pedigrees

Amina Bakhchane, Majida Charif, Sara Salime et al. · PLoS ONE · 2015 · 27 citations · Full text

Mendelian Disorder, Genetic Disorder, Medicine +14

Homozygous mutations in PJVK and MYO15A genes associated with non-syndromic hearing loss in Moroccan families

Sara Salime, Majida Charif, Amale Bousfiha et al. · International Journal of Pediatric Otorhinolaryngology · 2017 · 21 citations

Homozygous Mutations, Myo15a Genes, Genetic Disorder +10