Nabil Driss

A missense mutation in DCDC2 causes human recessive deafness DFNB66, likely by interfering with sensory hair cell and supporting cell cilia length regulation

M’hamed Grati, Imen Chakchouk, Qi Ma et al. · Human Molecular Genetics · 2015 · 97 citations · Full text

Genetics, Cytoskeleton, Disease Gene Identification +20

<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

Association of COL1A1 and TGFB1 Polymorphisms with Otosclerosis in a Tunisian Population

Ayda Khalfallah, Isabelle Schrauwen, Malek Mnejja et al. · Annals of Human Genetics · 2011 · 31 citations

Genome-wide Association Study, Autoimmune Disease, Otic Capsule +15

A Novel Autosomal Recessive Non-Syndromic Deafness Locus, &lt;i&gt;DFNB66&lt;/i&gt;, Maps to Chromosome 6p21.2-22.3 in a Large Tunisian Consanguineous Family

Abdelaziz Tlili, Minna Männikkö, Ilhem Charfedine et al. · Human Heredity · 2005 · 28 citations