Additional file 1: Table S1. of Association of a rare NOTCH4 coding variant with systemic sclerosis: a family-based whole exome sequencing study
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https://figshare.com/articles/dataset/Additional_file_1_Table_S1_of_Association_of_a_rare_NOTCH4_coding_variant_with_systemic_sclerosis_a_family-based_whole_exome_sequencing_study/4401365
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资源简介：
Table of rare coding variants segregating with the SSc/scleroderma phenotype. (XLS 27 kb)
创建时间：
2017-03-10
