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Article Source: Whole Exome Sequencing Identifies New Causative Mutations in Tunisian Families with Non-Syndromic Deafness
Riahi Z, Bonnet C, Zainine R, Louha M, Bouyacoub Y, et al. (2014) Whole Exome Sequencing Identifies New Causative Mutations in Tunisian Families with Non-Syndromic Deafness. PLOS ONE 9(6): e99797. https://doi.org/10.1371/journal.pone.0099797

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