Additional file 8: 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://springernature.figshare.com/articles/Additional_file_8_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/7047290
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Table S4. and lists candidates for exclusion - genes with predicted pathogenic variants in many exome projects or across multiple families exhibiting a variety of phenotypes. This list consists of the genes in Supplementary Tables S1 and S2 from [29]. (XLS 46 kb)
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figshare
创建时间：
2018-09-05
