MOESM5 of Post-lingual non-syndromic hearing loss phenotype: a polygenic case with 2 biallelic mutations in MYO15A and MITF
收藏Figshare2020-01-02 更新2026-04-28 收录
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https://figshare.com/articles/dataset/MOESM5_of_Post-lingual_non-syndromic_hearing_loss_phenotype_a_polygenic_case_with_2_biallelic_mutations_in_MYO15A_and_MITF/11497773
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Additional file 5: Table S5. Filtering results from whole exome sequencing for patient II.6 showing only homozygous mutations with a MAF < 5%.
创建时间：
2020-01-02
