MOESM5 of Post-lingual non-syndromic hearing loss phenotype: a polygenic case with 2 biallelic mutations in MYO15A and MITF
收藏NIAID Data Ecosystem2026-03-11 收录
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资源简介：
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
