Sa.76. Ipex Syndrome with Normal FOXP3 Coding Region Sequences But Diminished FOXP3 Transcription and Translation: An Implied FOXP3 Regulatory Gene Defect
Frederick Schaffer, Joe Cochran, L. Key, Talal Chatila, S. Anover, M. Hackett, Hans Ochs, Troy TorgersonVolume:
119
Year:
2006
Language:
english
Pages:
1
DOI:
10.1016/j.clim.2006.04.308
File:
PDF, 53 KB
english, 2006