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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
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 |