Schaffer, F., Cochran, J., Key, L., Chatila, T., Anover, S., Hackett, M., . . . Torgerson, T. (2006). Sa.76. Ipex Syndrome with Normal FOXP3 Coding Region Sequences But Diminished FOXP3 Transcription and Translation: An Implied FOXP3 Regulatory Gene Defect. Clinical Immunology, 119, S131. https://doi.org/10.1016/j.clim.2006.04.308
Chicago Style (17th ed.) CitationSchaffer, Frederick, Joe Cochran, L. Key, Talal Chatila, S. Anover, M. Hackett, Hans Ochs, and Troy Torgerson. "Sa.76. Ipex Syndrome with Normal FOXP3 Coding Region Sequences But Diminished FOXP3 Transcription and Translation: An Implied FOXP3 Regulatory Gene Defect." Clinical Immunology 119 (2006): S131. https://doi.org/10.1016/j.clim.2006.04.308.
MLA (9th ed.) CitationSchaffer, Frederick, et al. "Sa.76. Ipex Syndrome with Normal FOXP3 Coding Region Sequences But Diminished FOXP3 Transcription and Translation: An Implied FOXP3 Regulatory Gene Defect." Clinical Immunology, vol. 119, 2006, p. S131, https://doi.org/10.1016/j.clim.2006.04.308.