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Whole exome sequencing identifies new causative mutations in Tunisian families with non-syndromic deafness.PLoS ONE, 2014, 9 (6), pp.e99797. ⟨10.1371/journal.pone.0099797⟩
Journal articles
pasteur-01060192v1
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Update of the spectrum of GJB2 gene mutations in Tunisian families with autosomal recessive nonsyndromic hearing loss.Gene, 2013, 525 (1), pp.1-4. ⟨10.1016/j.gene.2013.04.078⟩
Journal articles
pasteur-00861409v1
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