ADRA2A and IRX1 are putative risk genes for Raynaud's phenomenon. (2023)

First Author: Hartmann S
Attributed to:  Multimorbidity Mechanism and Therapeutics Research Collaborative funded by SPF

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1038/s41467-023-41876-5

PubMed Identifier: 37828025

Publication URI: http://europepmc.org/abstract/MED/37828025

Type: Journal Article/Review

Volume: 14

Parent Publication: Nature communications

Issue: 1

ISSN: 2041-1723