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MOESM2 of Post-lingual non-syndromic hearing loss phenotype: a polygenic case with 2 biallelic mutations in MYO15A and MITF

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posted on 2020-01-03, 04:56 authored by Athar Khalil, Samer Karroum, Rana Barake, Gabriel Dunya, Samer Abou-Rizk, Amina Kamar, Georges Nemer, Marc Bassim
Additional file 2: Table S2. Filtering results from whole exome sequencing for patient II.5 using the 150 genes panel from Supplementary Table 1

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