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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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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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