MOESM2 of Post-lingual non-syndromic hearing loss phenotype: a polygenic case with 2 biallelic mutations in MYO15A and MITF
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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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Athar Khalil创建时间：
2020-01-03
