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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,

