Houria Dhouib

Identification of two new mutations in the GPR98 and the PDE6B genes segregating in a Tunisian family

Mounira Hmani‐Aifa, Z. Benzina, Fareeha Zulfiqar et al. · European Journal of Human Genetics · 2008 · 61 citations · Full text

New Mutations, Allelic Variant, Genetic Disorder +9

<i>TMC1</i> but Not <i>TMC2</i> Is Responsible for Autosomal Recessive Nonsyndromic Hearing Impairment in Tunisian Families

Abdelaziz Tlili, Imen Ben Rebeh, Mounira Hmani‐Aifa et al. · Audiology and Neurotology · 2008 · 59 citations

Screening of the <i>DFNB3</i> Locus: Identification of Three Novel Mutations of <i>MYO15A</i> Associated with Hearing Loss and Further Suggestion for Two Distinctive Genes on This Locus

Hanen Belguith, Mounira Hmani‐Aifa, Houria Dhouib et al. · Genetic Testing and Molecular Biomarkers · 2009 · 40 citations

Genetics, Pathology, Molecular Genetics +19

Mutation in gap and tight junctions in patients with non-syndromic hearing loss

Hanen Belguith, Abdelaziz Tlili, Houria Dhouib et al. · Biochemical and Biophysical Research Communications · 2009 · 17 citations

Non-syndromic Hearing Loss, Audiology, Hearing Disorders +6

Segregation of a new mutation in SLC26A4 and p.E47X mutation in GJB2 within a consanguineous Tunisian family affected with Pendred syndrome

Mariem Ben Saïd, Houria Dhouib, Z. Benzina et al. · International Journal of Pediatric Otorhinolaryngology · 2012 · 14 citations

New Mutation, Mendelian Disorder, P.e47x Mutation +9