Imen Ben Rebeh

<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

A novel dominant mutation in SIX1, affecting a highly conserved residue, result in only auditory defects in humans

Mohamed Ali Mosrati, B. Hammami, Imen Ben Rebeh et al. · European Journal of Medical Genetics · 2011 · 32 citations

Biology, Developmental Anomaly, Genetic Disorder +14

Localization of a Novel Autosomal Recessive Non‐syndromic Hearing Impairment Locus <i>DFNB63</i> to Chromosome 11q13.3‐q13.4

Abdelaziz Tlili, Saber Masmoudi, H. Dhouib et al. · Annals of Human Genetics · 2006 · 23 citations

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

Reinforcement of a minor alternative splicing event in MYO7A due to a missense mutation results in a mild form of retinopathy and deafness.

Imen Ben Rebeh, Madeleine Morinière, Leila Ayadi et al. · PubMed · 2010 · 16 citations