Sa.76. Ipex Syndrome with Normal FOXP3 Coding Region Sequences But Diminished FOXP3 Transcription and Translation: An Implied FOXP3 Regulatory Gene Defect

✍ Scribed by Frederick Schaffer; Joe Cochran; L. Key; Talal Chatila; S. Anover; M. Hackett; Hans Ochs; Troy Torgerson

• Book ID: 116366597
• Publisher: Elsevier Science
• Year: 2006
• Tongue: English
• Weight: 53 KB
• Volume: 119
• Category: Article
• ISSN: 1090-2341
• DOI: 10.1016/j.clim.2006.04.308