- Title
- RAC2 loss-of-function mutation in 2 siblings with characteristics of common variable immunodeficiency
- Creators - without role
- Omar K. Alkhairy - King Abdulaziz Medical CityNima Rezaei - Tehran University of Medical SciencesRobert R. Graham - GenentechHassan Abolhassani - Tehran University of Medical SciencesStephan Borte - Karolinska InstitutetKjell Hultenby - Karolinska University HospitalChenglin Wu - Karolinska University HospitalAsghar Aghamohammadi - Children's Medical CenterDavid A. Williams - Harvard UniversityTimothy W. Behrens - GenentechLennart Hammarstrom - Karolinska InstitutetQiang Pan-Hammarstrom - Karolinska University Hospital
- Publication Details
- Journal of allergy and clinical immunology, Vol.135(5), pp.1380-1384.e5
- Publisher
- Elsevier
- Number of pages
- 10
- Grant note
- 242551 / European Research Council; European Research Council (ERC); European Commission R01DK062757 / NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES; United States Department of Health & Human Services; National Institutes of Health (NIH) - USA; NIH National Institute of Diabetes & Digestive & Kidney Diseases (NIDDK) R01 DK062757; 5R01DK062757-12 / NIDDK NIH HHS; United States Department of Health & Human Services; National Institutes of Health (NIH) - USA; NIH National Institute of Diabetes & Digestive & Kidney Diseases (NIDDK)
- Identifiers
- 9921368508331
- Academic Unit
- King Abdulaziz University; King Saud Bin Abdulaziz University for Health Sciences
- Language
- English
- Resource Type
- Journal article
Journal article
RAC2 loss-of-function mutation in 2 siblings with characteristics of common variable immunodeficiency
Journal of allergy and clinical immunology, Vol.135(5), pp.1380-1384.e5
01/05/2015
PMID: 25512081
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