CD137 deficiency because of two novel biallelic TNFRSF9 mutations in a patient presenting with severe EBV‐associated lymphoproliferative disease

OBJECTIVES: Increasing evidence indicates that some germline genetic mutations that impair pathways required for robust host immune surveillance against EBV infection may result in an extremely high susceptibility to EBV‐associated lymphoproliferative disease (EBV(+) LPD). TNFRSF9 encodes a vital co...

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Detalles Bibliográficos
Autores principales: Shen, Kefeng, Wang, Jiachen, Zhou, Kuangguo, Mu, Wei, Zhang, Meilan, Deng, Xinyue, Cai, Haodong, Zhang, Wei, Huang, Wei, Xiao, Min
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10153300/
https://www.ncbi.nlm.nih.gov/pubmed/37144041
http://dx.doi.org/10.1002/cti2.1448

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10153300/
https://www.ncbi.nlm.nih.gov/pubmed/37144041
http://dx.doi.org/10.1002/cti2.1448

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