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Acknowledgements
We kindly acknowledge Dr. Amy Pallor from Ann & Robert H Lurie Children’s Hospital of Chicago Division of Dermatology for hel** with the collection and culture of the patient’s fibroblasts for functional studies and Luisa Kamm and Tatiana Kochetkov from Dr. Casanova’s lab for technical support. We also acknowledge Dr. Kai Lee Yap’s Molecular Lab, also at Lurie Children’s, for their work on the whole genome research study performed for this case.
Funding
The Laboratory of Human Genetics of Infectious Diseases was supported by the Howard Hughes Medical Institute, the Rockefeller University, the St. Giles Foundation, the National Institutes of Health (NIH) (P01AI061093), the French National Research Agency (ANR) under the “Investments for the Future” program (ANR-10-IAHU-01), the French Foundation for Medical Research (FRM; EQU201903007798), the Square Foundation, Grandir—Fonds de solidarité pour l’enfance, the Fondation du Souffle, the SCOR Corporate Foundation for Science, Institut National de la Santé et de la Recherche Médicale (INSERM), and the University of Paris Cité.
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Gunderman, L.M., Asano, T., Casanova, JL. et al. Novel NF-kappa B Inhibitor Alpha Gain-of-Function Variant in an Infant with Lymphocytosis and Recurrent Serratia Bacteremia. J Clin Immunol 43, 1122–1126 (2023). https://doi.org/10.1007/s10875-023-01481-z
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DOI: https://doi.org/10.1007/s10875-023-01481-z