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Whole exome sequencing identifies mutations in Usher syndrome genes in profoundly deaf Tunisian patients

Author / Creator:Riahi, Zied ; Bonnet, Crystel ; Zainine, Rim ; Lahbib, Saida ; Bouyacoub, Yosra ; Bechraoui, Rym ; Marrakchi, Jihène ; Hardelin, Jean-Pierre ; Louha, Malek ; Largueche, Leila ; Ben Yahia, Salim ; Kheirallah, Moncef ; Elmatri, Leila ; Besbes, Ghazi ; Abdelhak, Sonia ; Petit, Christine

Publisher:United States: Public Library of Science

Journal title:PloS one, 2015-03, Vol.10 (3), p.e0120584-e0120584

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Whole exome sequencing identifies mutations in Usher syndrome genes in profoundly deaf Tunisian patients

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