MOESM3 of Post-lingual non-syndromic hearing loss phenotype: a polygenic case with 2 biallelic mutations in MYO15A and MITF
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https://figshare.com/articles/dataset/MOESM3_of_Post-lingual_non-syndromic_hearing_loss_phenotype_a_polygenic_case_with_2_biallelic_mutations_in_MYO15A_and_MITF/11497761
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资源简介：
Additional file 3: Table S3. Filtering results from whole exome sequencing for patient II.6 using the 150 genes panel from Supplementary Table 1
创建时间：
2020-01-02
