12881_2019_942_MOESM5_ESM.xls (38 kB)
MOESM5 of Post-lingual non-syndromic hearing loss phenotype: a polygenic case with 2 biallelic mutations in MYO15A and MITF
dataset
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 BassimAdditional file 5: Table S5. Filtering results from whole exome sequencing for patient II.6 showing only homozygous mutations with a MAF < 5%.
