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Additional file 1: of A novel pathogenic variant in OSBPL2 linked to hereditary late-onset deafness in a Mongolian family

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posted on 2019-03-20, 05:00 authored by Ningjin Wu, Husile Husile, Liqing Yang, Yaning Cao, Xing Li, Wenyan Huo, Haihua Bai, Yangjian Liu, Qizhu Wu
Table S1. The genome-wide analysis list. Table S2. Average coverage. Table S3. 127 genes panel of hereditary deafness(in BGI). (PDF 80 kb)

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National Natural Science Foundation of China

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