Primary Sjögren's syndrome and high type I interferon signalling in a kindred with C2 deficiency

Detalles Bibliográficos
Autores principales: Willemsen, Mathijs, Van Nieuwenhove, Erika, Seyed Tabib, Nasim Sadat, Staels, Frederik, Schrijvers, Rik, De Somer, Lien, Liston, Adrian, Humblet-Baron, Stephanie, Wouters, Carine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Letter to the Editor (Case report)
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8969662/
https://www.ncbi.nlm.nih.gov/pubmed/35368972
http://dx.doi.org/10.1093/rap/rkac018

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8969662/
https://www.ncbi.nlm.nih.gov/pubmed/35368972
http://dx.doi.org/10.1093/rap/rkac018

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