A rare polyadenylation signal mutation of theFOXP3gene (AAUAAA→AAUGAA) leads to the IPEX syndrome

✍ Scribed by 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

• Book ID: 105948950
• Publisher: Springer-Verlag
• Year: 2001
• Tongue: English
• Weight: 105 KB
• Volume: 53
• Category: Article
• ISSN: 0093-7711
• DOI: 10.1007/s002510100358