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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.
Journal articles
pasteur-01375019v1
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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.
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.
Journal articles
pasteur-01060192v1
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A novel frameshift mutation (c.405delC) in the GJB2 gene associated with autosomal recessive hearing loss in two Tunisian families.
Zied Riahi
,
Houda Chahed
,
Habib Jaafoura
,
Rim Zainine
,
Olfa Messaoud
,
et al.
Journal articles
pasteur-00861211v1
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Alpha-mannosidosis in Tunisian consanguineous families: Potential involvement of variants in GHR and SLC19A3 genes in the variable expressivity of cognitive impairment
Rahma Mkaouar
,
Zied Riahi
,
Cherine Charfeddine
,
Imen Chelly
,
Hela Boudabbous
,
et al.
Journal articles
pasteur-04072687v1
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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.
Journal articles
pasteur-03219630v1
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Compound heterozygosity for dominant and recessive GJB2 mutations in a Tunisian family and association with successful cochlear implant outcome.
Zied Riahi
,
Rim Zainine
,
Yosra Mellouli
,
Raja Hannachi
,
Yosra Bouyacoub
,
et al.
Journal articles
pasteur-00860772v1
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Update of the spectrum of GJB2 gene mutations in Tunisian families with autosomal recessive nonsyndromic hearing loss.
Zied Riahi
,
Hassen Hammami
,
Houyem Ouragini
,
Habib Messai
,
Rim Zainine
,
et al.
Journal articles
pasteur-00861409v1
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