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MOESM5 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 03.01.2020, 04:56 authored by Athar Khalil, Samer Karroum, Rana Barake, Gabriel Dunya, Samer Abou-Rizk, Amina Kamar, Georges Nemer, Marc Bassim
Additional file 5: Table S5. Filtering results from whole exome sequencing for patient II.6 showing only homozygous mutations with a MAF < 5%.

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