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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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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.
Journal articles
pasteur-03219641v1
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A homozygous MPZL2 deletion is associated with non syndromic hearing loss in a moroccan family
Ghita Amalou
,
Crystel Bonnet
,
Zied Riahi
,
Aymane Bouzidi
,
Soukaina Elrharchi
,
et al.
Journal articles
pasteur-03215242v1
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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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Novel Mutation in AIFM1 Gene Associated with X-Linked Deafness in a Moroccan Family
Soukaina Elrharchi
,
Zied Riahi
,
Sara Salime
,
Hicham Charoute
,
Lamiae Elkhattabi
,
et al.
Journal articles
pasteur-03219602v1
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A novel splice-site mutation in ATP6V0A4 gene in two brothers with distal renal tubular acidosis from a consanguineous Tunisian family
Majdi Nagara
,
Konstantinos Voskarides
,
Sahar Elouej
,
Apostolos Zaravinos
,
Zied Riahi
,
et al.
Journal articles
hal-01358526v1
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Specific aspects of consanguinity: some examples from the tunisian population.
Lilia Romdhane
,
Nizar Ben Halim
,
Insaf Rejeb
,
Rym Kefi
,
Yosra Bouyacoub
,
et al.
Journal articles
pasteur-01061190v1
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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.
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.
Journal articles
pasteur-03219646v1
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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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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.
Journal articles
pasteur-03219615v1
|
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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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