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...

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Vydáno v:Open Forum Infect Dis
Hlavní autoři: Cai, Yu Qing, Zhang, HangHu, Wang, Xiang Zhi, Xu, ChengYun, Chao, Yun Qi, Shu, YingYing, Tang, Lan Fang
Médium: Artigo
Jazyk:Inglês
Vydáno: Oxford University Press 2020
Témata:
Novel ID Cases
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC7452370/
https://ncbi.nlm.nih.gov/pubmed/32875002
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/ofid/ofaa314
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