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Structure: Internal structure identifier : 1059120
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Whole exome sequencing identifies mutations in Usher syndrome genes in profoundly deaf Tunisian patients.

Zied Riahi , Crystel Bonnet , Rim Zainine , Saida Lahbib , Yosra Bouyacoub , et al.
PLoS ONE, 2015, 10 (3), pp.e0120584. ⟨10.1371/journal.pone.0120584⟩
Journal articles pasteur-01221041v1
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Whole exome sequencing identifies new causative mutations in Tunisian families with non-syndromic deafness.

Zied Riahi , Crystel Bonnet , Rim Zainine , Malek Louha , Yosra Bouyacoub , et al.
PLoS ONE, 2014, 9 (6), pp.e99797. ⟨10.1371/journal.pone.0099797⟩
Journal articles pasteur-01060192v1

Specific aspects of consanguinity: some examples from the tunisian population.

Lilia Romdhane , Nizar Ben Halim , Insaf Rejeb , Rym Kefi , Yosra Bouyacoub , et al.
Human Heredity, 2014, 77 (1-4), pp.167-74. ⟨10.1159/000362167⟩
Journal articles pasteur-01061190v1

A novel mutation in SLITRK6 causes deafness and myopia in a Moroccan family

Sara Salime , Zied Riahi , Soukaina Elrharchi , Lamiae Elkhattabi , Hicham Charoute , et al.
Gene, 2018, 659, pp.89-92. ⟨10.1016/j.gene.2018.03.042⟩
Journal articles pasteur-03219641v1

Estimation of Recent and Ancient Inbreeding in a Small Endogamous Tunisian Community Through Genomic Runs of Homozygosity

Nizar Ben Halim , Majdi Nagara , Béatrice Regnault , Sana Hsouna , Khaled Lasram , et al.
Annals of Human Genetics, 2015, 79 (6), pp.402 - 417. ⟨10.1111/ahg.12131⟩
Journal articles pasteur-01375019v1
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Mutations in CDC14A, Encoding a Protein Phosphatase Involved in Hair Cell Ciliogenesis, Cause Autosomal-Recessive Severe to Profound Deafness

Sedigheh Delmaghani , Asadollah Aghaie , Yosra Bouyacoub , Hala El Hachmi , Crystel Bonnet , et al.
American Journal of Human Genetics, 2016, 98 (6), pp.1266 - 1270. ⟨10.1016/j.ajhg.2016.04.015⟩
Journal articles hal-01329650v1
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A novel PEX1 mutation in a Moroccan family with Zellweger spectrum disorders

Amale Bousfiha , Amina Bakhchane , Hicham Charoute , Zied Riahi , Khalid Snoussi , et al.
Human Genome Variation, 2017, 4 (1), pp.17009. ⟨10.1038/hgv.2017.9⟩
Journal articles pasteur-03219646v1

A Tunisian family with a novel mutation in the gene CYP 4F22 for lamellar ichthyosis and co‐occurrence of hearing loss in a child due to mutation in the SLC 26A4 gene

Marwa Sayeb , Zied Riahi , Nadia Laroussi , Crystel Bonnet , Lilia Romdhane , et al.
International Journal of Dermatology, 2019, 58 (12), pp.1439-1443. ⟨10.1111/ijd.14452⟩
Journal articles pasteur-03219630v1

Further Evidence for the Implication of the MET Gene in Non-Syndromic Autosomal Recessive Deafness

Amale Bousfiha , Zied Riahi , Lamiae Elkhattabi , Amina Bakhchane , Hicham Charoute , et al.
Human Heredity, 2020, 84 (3), pp.109-116. ⟨10.1159/000503450⟩
Journal articles pasteur-03219615v1