Volume 123, Issue 5 , Pages 1170-1173.e3, May 2009
Clinical and genetic diagnosis of warts, hypogammaglobulinemia, infections, and myelokathexis syndrome in 10 patients
No abstract is available. To read the body of this article, please view the Full Text online.
Supported by grants from Telethon GGP07134, Fondazione Cariplo NOBEL grant, EU grant FP7 HLH-cure (project no. 201461), e-rare EU grant, Rare Diseases-ISS project, PRIN 2007 no. 2007ACZMMZ_005, the Swedish Science Council, and the EU FP7 grant Euro-Gene-Scan (project number 223293).
Disclosure of potential conflict of interest: C. I. E. Smith has received research support from the Swedish Science Council, the Swedish Cancer Society, and the European Union. L. D. Notarangelo is on a scientific advisory board for the Immune Disease Institute and is Co-chair of International Union of Immunological Societies' Committee of Primary Immunodeficiencies. R. Badolato has received research support from the European Union, Telethon Italy, and the Italian Ministry of Research. The rest of the authors have declared that they have no conflict of interest.
PII: S0091-6749(09)00168-7
doi:10.1016/j.jaci.2008.12.1133
© 2009 American Academy of Allergy, Asthma & Immunology. Published by Elsevier Inc. All rights reserved.
Volume 123, Issue 5 , Pages 1170-1173.e3, May 2009
