Autoimmune lymphoproliferative syndrome caused by a homozygous FasL mutation that disrupts FasL assembly - 07/01/16

| This study was supported by a Boston Children's Hospital Investigatorship Award (M.J.M.) and grants from the Jeffrey Modell Foundation and the Dubai Harvard Foundation for Medical Research. The funding sources were not involved in the study design, in the collection, analysis, and interpretation of data, in the writing of the report, and in the decision to submit the article for publication. |
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| Disclosure of potential conflict of interest: J. Chou has received research support from the Jeffrey Modell Foundation and the National Institutes of Health (NIH) and is employed by Boston Children's Hospital. S.-Y. Pai has received research support from the NIH (grants pending) and is employed by Boston Children's Hospital (salary including funds from the Translational Investigator Service Award, from the Venture Philanthropy Network). L. D. Notarangelo has received research support from the NIH and the March of Dimes; is a board member for the Journal of Allergy and Clinical Immunology and the Journal of Clinical Immunology; is a member of the Data Safety Monitoring Board for Novimmune; is employed by Boston Children's Hospital; and has received royalties from UpToDate and Garland. M. J. Massaad has received research support from Boston Children's Hospital (Young Investigatorship Award). The rest of the authors declare that they have no relevant conflicts of interest. |
Vol 137 - N° 1
P. 324 - janvier 2016 Retour au numéroBienvenue sur EM-consulte, la référence des professionnels de santé.
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