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

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

Abstract 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. Me...

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Bibliographic Details
Main Authors: Liwen Tan, Yunfei An, Qin Yang, Haiping Yang, Gaofu Zhang, Qiu Li, Mo Wang
Format: Article
Language:English
Published: Wiley 2022-06-01
Series:Molecular Genetics & Genomic Medicine
Subjects:
FOXP3
IPEX syndrome
membranous nephropathy
Online Access:https://doi.org/10.1002/mgg3.1945

Internet

https://doi.org/10.1002/mgg3.1945

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