Additional file 1: Table S1. of Association of a rare NOTCH4 coding variant with systemic sclerosis: a family-based whole exome sequencing study
收藏DataCite Commons2024-12-16 更新2024-07-27 收录
下载链接：
https://springernature.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/4401365/1
下载链接
链接失效反馈官方服务：
资源简介：
Table of rare coding variants segregating with the SSc/scleroderma phenotype. (XLS 27 kb)
提供机构：
Figshare
创建时间：
2017-12-19
