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Whole exome sequencing identifies mutations in Usher syndrome genes in profoundly deaf Tunisian patients.PLoS ONE, 2015, 10 (3), pp.e0120584. ⟨10.1371/journal.pone.0120584⟩
Journal articles
pasteur-01221041v1
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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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Mutations in CDC14A, Encoding a Protein Phosphatase Involved in Hair Cell Ciliogenesis, Cause Autosomal-Recessive Severe to Profound DeafnessAmerican Journal of Human Genetics, 2016, 98 (6), pp.1266 - 1270. ⟨10.1016/j.ajhg.2016.04.015⟩
Journal articles
hal-01329650v1
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