Large deletions and point mutations involving the dedicator of cytokinesis 8 (DOCK8) in the autosomal-recessive form of hyper-IgE syndrome
Top Cited Papers
Open Access
- 1 December 2009
- journal article
- research article
- Published by Elsevier in Journal of Allergy and Clinical Immunology
- Vol. 124 (6) , 1289-1302.e4
- https://doi.org/10.1016/j.jaci.2009.10.038
Abstract
No abstract availableKeywords
This publication has 27 references indexed in Scilit:
- Combined Immunodeficiency Associated withDOCK8MutationsNew England Journal of Medicine, 2009
- Isolated populations and complex disease gene identificationGenome Biology, 2008
- STAT3Mutations in the Hyper-IgE SyndromeNew England Journal of Medicine, 2007
- The Hyper IgE Syndrome and Mutations in TYK2Immunity, 2007
- Human Tyrosine Kinase 2 Deficiency Reveals Its Requisite Roles in Multiple Cytokine Signals Involved in Innate and Acquired ImmunityImmunity, 2006
- Hyper‐IgE syndromesImmunological Reviews, 2005
- Detection of large-scale variation in the human genomeNature Genetics, 2004
- Autosomal recessive hyperimmunoglobulin E syndrome: a distinct disease entityThe Journal of Pediatrics, 2004
- Genetic Linkage of Hyper-IgE Syndrome to Chromosome 4American Journal of Human Genetics, 1999
- Hyper-IgE Syndrome with Recurrent Infections — An Autosomal Dominant Multisystem DisorderNew England Journal of Medicine, 1999