共 50 条
- [13] A rare polyadenylation signal mutation of the FOXP3 gene (AAUAAA→AAUGAA) leads to the IPEX syndrome Immunogenetics, 2001, 53 : 435 - 439
- [15] Extremely Early Onset IPEX Syndrome Caused by a Novel Small Exonic Deletion in FOXP3 JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION, 2016, 63 (05): : E119 - E120
- [16] FOXP3 Forkhead Domain Mutation and Regulatory T Cells in the IPEX Syndrome NEW ENGLAND JOURNAL OF MEDICINE, 2009, 361 (17): : 1710 - 1713