共 2 条
[1]
A functional polymorphism in the promoter/enhancer region of the FOXP3/Scurfin gene associated with type 1 diabetes[J] Wafaa M. Bassuny;Kenji Ihara;Yuka Sasaki;Ryuichi Kuromaru;Hitoshi Kohno;Nobuo Matsuura;Toshiro Hara Immunogenetics 2003,
[2]
A rare polyadenylation signal mutation of the FOXP3 gene (AAUAAA→AAUGAA) leads to the IPEX syndrome[J] Craig L. Bennett;Mary E. Brunkow;Fred Ramsdell;Kathy C. O'Briant;Qili Zhu;Ramsay L. Fuleihan;Ann O. Shigeoka;Hans D. Ochs;Phillip F. Chance Immunogenetics 2001,

