Additional file 2: of Whole exome sequencing identified a novel truncation mutation in the NHS gene associated with Nance-Horan syndrome
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https://figshare.com/articles/dataset/Additional_file_2_of_Whole_exome_sequencing_identified_a_novel_truncation_mutation_in_the_NHS_gene_associated_with_Nance-Horan_syndrome/7587500
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Detailed annotation of the retained 129 variants. ACMG standards were used for variant classification, and the OMIM database was used for priority analysis of the phenotype matching. (XLSX 47 kb)
创建时间：
2019-01-15
