Additional file 1: of Novel digenic inheritance of PCDH15 and USH1G underlies profound non-syndromic hearing impairment
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Supplementary data associated with this manuscript consists of Table S1. Variants of interest identified by exome sequencing. This list includes variants in this study that were tested for segregation. Annotations and population frequencies are listed. (XLSX 12 kb).
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figshare创建时间：
2019-10-25
