Publications by authors named "Sara Salime"

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Genetics of prelingual isolated deafness and Usher syndrome in the Maghreb and Jordan: Harnessing the potential of homozygosity.
Zied Riahi, Sophie Boucher, Samia Abdi, Fabienne Wong Jun Tai, Amrit Singh-Estivalet, Sara Salime

Proc Natl Acad Sci U S A· December 2025

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Novel Mutation in AIFM1 Gene Associated with X-Linked Deafness in a Moroccan Family.
Soukaina Elrharchi, Zied Riahi, Sara Salime, Hicham Charoute, Lamiae Elkhattabi

Hum Hered· November 2021

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Two novel homozygous missense mutations identified in the BSND gene in Moroccan patients with Bartter's syndrome.
Soukaina Elrharchi, Zied Riahi, Sara Salime, Halima Nahili, Hassan Rouba

Int J Pediatr Otorhinolaryngol· October 2018

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A novel mutation in SLITRK6 causes deafness and myopia in a Moroccan family.
Sara Salime, Zied Riahi, Soukaina Elrharchi, Lamiae Elkhattabi, Hicham Charoute

Gene· June 2018

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Homozygous mutations in PJVK and MYO15A genes associated with non-syndromic hearing loss in Moroccan families.
Sara Salime, Majida Charif, Amale Bousfiha, Soukaina Elrharchi, Amina Bakhchane

Int J Pediatr Otorhinolaryngol· October 2017

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Update of the spectrum of GJB2 gene mutations in 152 Moroccan families with autosomal recessive nonsyndromic hearing loss.
Amina Bakhchane, Amale Bousfiha, Hicham Charoute, Sara Salime, Mustapha Detsouli

Eur J Med Genet· June 2016

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Recessive TBC1D24 Mutations Are Frequent in Moroccan Non-Syndromic Hearing Loss Pedigrees.
Amina Bakhchane, Majida Charif, Sara Salime, Redouane Boulouiz, Halima Nahili

PLoS One· May 2016

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A novel mutation of AFG3L2 might cause dominant optic atrophy in patients with mild intellectual disability.
Majida Charif, Agathe Roubertie, Sara Salime, Sonia Mamouni, Cyril Goizet

Front Genet· November 2015

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