Additional file 7: of Whole exome sequencing in adult-onset hearing loss reveals a high load of predicted pathogenic variants in known deafness-associated genes and identifies new candidate genes
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https://figshare.com/articles/dataset/Additional_file_7_of_Whole_exome_sequencing_in_adult-onset_hearing_loss_reveals_a_high_load_of_predicted_pathogenic_variants_in_known_deafness-associated_genes_and_identifies_new_candidate_genes/7047275
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Table S3. listing genes reported to underlie deafness in humans and/or mice. (XLS 45 kb)
表S3：列出了据报道可在人类和/或小鼠中诱发耳聋的基因（XLS格式，45千字节）
创建时间：
2018-09-05
