12891_2016_1320_MOESM1_ESM.xls (27.5 kB)
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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posted on 2016-11-09, 05:00 authored by Christopher Cardinale, Dong Li, Lifeng Tian, John Connolly, Michael March, Cuiping Hou, Fengxiang Wang, James Snyder, Cecilia Kim, Rosetta Chiavacci, Patrick Sleiman, Jon Burnham, Hakon HakonarsonTable of rare coding variants segregating with the SSc/scleroderma phenotype. (XLS 27 kb)
