Identification of Critical Transcriptomic Signaling Pathways in Patients with H Syndrome and Rosai-Dorfman Disease

Biallelic mutations in SLC29A3 cause histiocytosis-lymphadenopathy plus syndrome, also known as H syndrome (HS). HS is a complex disorder, with ~ 25% of patients developing autoinflammatory complications consisting of unexplained fevers, persistently elevated inflammatory markers, and unusual lympha...

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Detalles Bibliográficos
Autores principales: Lara-Reyna, Samuel, Poulter, James A., Vasconcelos, Elton J.R., Kacar, Mark, McDermott, Michael F., Tooze, Reuben, Doffinger, Rainer, Savic, Sinisa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2020
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7858559/
https://www.ncbi.nlm.nih.gov/pubmed/33284430
http://dx.doi.org/10.1007/s10875-020-00932-1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7858559/
https://www.ncbi.nlm.nih.gov/pubmed/33284430
http://dx.doi.org/10.1007/s10875-020-00932-1

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