Broadening our understanding of genetic risk for scleroderma/systemic sclerosis by querying the chromatin architecture surrounding the risk haplotypes

• Prif Awduron: Kerry E. Poppenberg (Awdur), Vincent M. Tutino (Awdur), Evan Tarbell (Awdur), James N. Jarvis (Awdur)
• Fformat: Llyfr
• Cyhoeddwyd: BMC, 2021-04-01T00:00:00Z.
• Pynciau: article
• Mynediad Ar-lein: Connect to this object online.

Abstract Background Genetic variants in the human leukocyte antigen (HLA) locus contribute to the risk for developing scleroderma/systemic sclerosis (SSc). However, there are other replicated loci that also contribute to genetic risk for SSc, and it is unknown whether genetic risk in these non-HLA l...