Mohamed Drira

The autosomal recessive isolated deafness, DFNB2, and the Usher 1B syndrome are allelic defects of the myosin-VIIA gene

Dominique Weil, Polonca Küssel, Stéphane Blanchard et al. · Nature Genetics · 1997 · 427 citations

Life Sciences, Genetics, Molecular Genetics +13

A human gene responsible for neurosensory, non-syndromic recessive deafness is a candidate homologue of the mouse <i>sh-1</i> gene

Parry Guilford, Hamadi Ayadi, Stéphane Blanchard et al. · Human Molecular Genetics · 1994 · 127 citations

Life Sciences, Genetics, Molecular Genetics +10

A novel locus for Usher syndrome type II, USH2B, maps to chromosome 3 at p23–24.2

Mounira Hmani‐Aifa, Abdelmonem Ghorbel, Amel Boulila‐Elgaied et al. · European Journal of Human Genetics · 1999 · 85 citations

Life Sciences, Genetics, Molecular Genetics +10

Novel missense mutations of TMPRSS3 in two consanguineous Tunisian families with non-syndromic autosomal recessive deafness

Saber Masmoudi, Stylianos E. Antonarakis, Torsten Schwede et al. · Human Mutation · 2001 · 76 citations

Life Sciences, Genetics, Molecular Genetics +16

Pendred syndrome: Phenotypic variability in two families carrying the samePDS missense mutation

Saber Masmoudi, Ilhem Charfedine, Mounira Hmani‐Aifa et al. · American Journal of Medical Genetics · 2000 · 72 citations

Medicine, Genetics, Molecular Genetics +17