A novel missense mutation of FOXP3 causes immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome in a Chinese child

OBJECTIVE: To investigate variation of FOXP3 and it's expression in male children presented with severe and early-onset enteropathy, rash with or without insulin-dependent diabetes mellitus (IDDM)

Détails bibliographiques
Publié dans:Zhonghua er ke za zhi = Chinese journal of pediatrics. - 1960. - 47(2009), 11 vom: 18. Nov., Seite 824-8
Auteur principal: An, Yun-fei (Auteur)
Autres auteurs: Zhao, Xiao-dong, Xu, Feng, Yang, Xi-qiang
Format: Article
Langue:Chinese
Publié: 2009
Accès à la collection:Zhonghua er ke za zhi = Chinese journal of pediatrics
Sujets:Case Reports English Abstract Journal Article Research Support, Non-U.S. Gov't FOXP3 protein, human Forkhead Transcription Factors