Get started
Author

Soukaina Elrharchi

Observed name: S. Elrharchi
OpenAlex ID: A5091780074
Homozygous mutations in PJVK and MYO15A genes associated with non-syndromic hearing loss in Moroccan families
2017 · Sara Salime, Majida Charif, et al. · International Journal of Pediatric Otorhinolaryngology · 20
A homozygous MPZL2 deletion is associated with non syndromic hearing loss in a moroccan family
2020 · Ghita Amalou, Crystel Bonnet, et al. · International Journal of Pediatric Otorhinolaryngology · 9
Novel Mutation in AIFM1 Gene Associated with X-Linked Deafness in a Moroccan Family
2020 · Soukaina Elrharchi, Zied Riahi, et al. · Human Heredity · 8
A novel mutation in SLITRK6 causes deafness and myopia in a Moroccan family
2018 · Sara Salime, Zied Riahi, et al. · Gene · 7
Two novel homozygous missense mutations identified in the BSND gene in Moroccan patients with Bartter's syndrome
2018 · Soukaina Elrharchi, Zied Riahi, et al. · International Journal of Pediatric Otorhinolaryngology · 6
Intra-familial phenotypic variability in a Moroccan family with hearing loss and palmoplantar keratoderma (PPK)
2016 · A. Bousfiha, A. Bakhchane, et al. · Current Research in Translational Medicine · 4
Genetics of prelingual isolated deafness and Usher syndrome in the Maghreb and Jordan: Harnessing the potential of homozygosity
2025 · Zied Riahi, Sophie Boucher, et al. · Proceedings of the National Academy of Sciences · 1
PDF
Works count: 7
Citation count: 55
H-index: 5
I10-index: 1
Year
Topic
Type