MOESM3 of Post-lingual non-syndromic hearing loss phenotype: a polygenic case with 2 biallelic mutations in MYO15A and MITF
收藏数据链接：
官方服务：
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
提供机构：
figshare创建时间：
2020-01-03
