Sa.76. Ipex Syndrome with Normal FOXP3 Coding Region Sequences But Diminished FOXP3 Transcription and Translation: An Implied FOXP3 Regulatory Gene Defect - Schaffer, Frederick; Cochran, Joe; Key, L.; Chatila, Talal; Anover, S.; Hackett, M.; Ochs, Hans; Torgerson, Troy (Clinical Immunology, 2006)