The clinical and laboratory spectrum of dedicator of cytokinesis 8 immunodeficiency syndrome in patients with a unique mutation-Reference-Cited by-同舟云学术

The clinical and laboratory spectrum of dedicator of cytokinesis 8 immunodeficiency syndrome in patients with a unique mutation

Published:2017-01-10 Issue:3 Volume:65 Page:651-657
ISSN:0257-277X
Container-title:Immunologic Research
language:en
Short-container-title:Immunol Res

Author:

Broides Arnon,Mandola Amarilla B,Levy Jacov,Yerushalmi Baruch,Pinsk Vered,Eldan Michal,Shubinsky George,Hadad Nurit,Levy Rachel,Nahum Amit,Ben-Harosh Miriam,Lev Atar,Simon Amos,Somech Raz

Publisher

Springer Science and Business Media LLC

Subject

Immunology

Link

http://link.springer.com/article/10.1007/s12026-016-8883-x/fulltext.html

Reference31 articles.

1. Zhang Q et al. Combined immunodeficiency associated with DOCK8 mutations. N Engl J Med. 2009;361:2046–55.

2. Engelhardt KR et al. Large deletions and point mutations involving the dedicator of cytokinesis 8 (DOCK8) in the autosomal-recessive form of hyper-IgE syndrome. J Allergy Clin Immunol. 2009;124:1289–302.e4.

3. Aydin SE et al. DOCK8 deficiency: clinical and immunological phenotype and treatment options—a review of 136 patients. J Clin Immunol. 2015;35:189–98. doi: 10.1007/s10875-014-0126-0 .

4. Zhang Q et al. Genetic, clinical, and laboratory markers for DOCK8 immunodeficiency syndrome. Dis Markers. 2010;29:131–9.

5. Crawford G et al. DOCK8 is critical for the survival and function of NKT cells. Blood. 2013;122(12):2052–61.

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