ADRA2A and IRX1 are putative risk genes for Raynaud’s phenomenon

Raynaud’s phenomenon (RP) is a common vasospastic disorder that causes severe pain and ulcers, but despite its high reported heritability, no causal genes have been robustly identified. We conducted a genome-wide association study including 5,147 RP cases and 439,294 controls, based on diagnoses fro...

Descripción completa

Detalles Bibliográficos
Autores principales: Hartmann, Sylvia, Yasmeen, Summaira, Jacobs, Benjamin M., Denaxas, Spiros, Pirmohamed, Munir, Gamazon, Eric R., Caulfield, Mark J., Hemingway, Harry, Pietzner, Maik, Langenberg, Claudia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10570309/
https://www.ncbi.nlm.nih.gov/pubmed/37828025
http://dx.doi.org/10.1038/s41467-023-41876-5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10570309/
https://www.ncbi.nlm.nih.gov/pubmed/37828025
http://dx.doi.org/10.1038/s41467-023-41876-5

Ejemplares similares