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Whole Exome Sequencing Identifies Mutations in Usher Syndrome Genes in Profoundly Deaf Tunisian Patients
- Zied Riahi,
- Crystel Bonnet,
- Rim Zainine,
- Saida Lahbib,
- Yosra Bouyacoub,
- Rym Bechraoui,
- Jihène Marrakchi,
- Jean-Pierre Hardelin,
- Malek Louha,
- Leila Largueche
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- Published: March 23, 2015
- https://doi.org/10.1371/journal.pone.0120584