A novel FOXP3 mutation in a Chinese child with IPEX‐associated membranous nephropathy

BACKGROUND: Immune dysregulation, polyendocrinopathy, enteropathy, X‐linked (IPEX) syndrome is a monogenic immunodeficiency disease caused by forkhead box protein3 (FOXP3) mutation. The kidney is commonly involved in IPEX syndrome, but there were few studies focusing on renal involvement. METHODS: W...

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Detalles Bibliográficos
Autores principales: Tan, Liwen, An, Yunfei, Yang, Qin, Yang, Haiping, Zhang, Gaofu, Li, Qiu, Wang, Mo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Clinical Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9184667/
https://www.ncbi.nlm.nih.gov/pubmed/35434975
http://dx.doi.org/10.1002/mgg3.1945

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9184667/
https://www.ncbi.nlm.nih.gov/pubmed/35434975
http://dx.doi.org/10.1002/mgg3.1945

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