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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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CYP1B1 gene mutations causing primary congenital glaucoma in Tunisia.Annals of Human Genetics, 2014, 78 (4), pp.255-63. ⟨10.1111/ahg.12069⟩
Journal articles
pasteur-01060119v1
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