Associated Papers
Analysis of ATP8B4 F436L Missense Variant in a Large Systemic Sclerosis Cohort.
López-Isac E et al.
Arthritis & Rheumatology (hoboken, N.j.), 2017
Identification of Rare Variants in ATP8B4 as a Risk Factor for Systemic Sclerosis by Whole-Exome Sequencing.
Gao L et al.
Arthritis & Rheumatology (hoboken, N.j.), 2016
A Novel Genetic Association With Systemic Sclerosis: The Utility of Whole-Exome Sequencing in Autoimmune Disease.
Aslibekyan S et al.
Arthritis & Rheumatology (hoboken, N.j.), 2016
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