A Novel RFXANK Mutation in a Chinese Child With MHC II Deficiency: Case Report and Literature Review

Major histocompatibility complex (MHC) II deficiency is a rare primary immunodeficiency disorder that is characterized by the deficiency of MHC class II molecules. The disease is caused by transcription factor mutations including class II transactivator (CIITA), regulatory factor X-5 (RFX5), RFX-ass...

Descripción completa

Detalles Bibliográficos
Autores principales: Cai, Yu Qing, Zhang, HangHu, Wang, Xiang Zhi, Xu, ChengYun, Chao, Yun Qi, Shu, YingYing, Tang, Lan Fang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Novel ID Cases
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7452370/
https://www.ncbi.nlm.nih.gov/pubmed/32875002
http://dx.doi.org/10.1093/ofid/ofaa314

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7452370/
https://www.ncbi.nlm.nih.gov/pubmed/32875002
http://dx.doi.org/10.1093/ofid/ofaa314

Ejemplares similares