DOCK8deficiency in six Iranian patients-Reference-Cited by-同舟云学术

DOCK8deficiency in six Iranian patients

Published:2016-05-17 Issue:6 Volume:4 Page:593-600
ISSN:2050-0904
Container-title:Clinical Case Reports
language:en
Short-container-title:Clin Case Rep

Author:

Saghafi Shiva¹,Pourpak Zahra¹²,Nussbaumer Franziska³,Fazlollahi Mohammad Reza¹,Houshmand Massoud⁴,Hamidieh Amir Ali⁵,Bemanian Mohammad Hassan⁶,Nabavi Mohammad⁶,Parvaneh Nima²,Grimbacher Bodo³,Moin Mostafa¹²,Glocker Cristina³

Affiliation:

1. Immunology; Asthma and Allergy Research Institute; Tehran University of Medical Sciences; Tehran Iran

2. Departments of Immunology and Allergy; Children Medical Center; Tehran University of Medical Sciences; Tehran Iran

3. Centre for Chronic Immunodeficiency (CCI); University Medical Center Freiburg and University of Freiburg; Freiburg Germany

4. Department of Medical Genetics; National Institute for Genetic Engineering and Biotechnology; Tehran Iran

5. Hematology-Oncology and Stem Cell Transplantation Research Center; Tehran University of Medical Sciences; Tehran Iran

6. Department of Allergy and Clinical Immunology Rasoul-e-Akram Hospital; Iran University of Medical Sciences; Tehran Iran

Funder

Collaboration of Tehran University of Medical Sciences

German Federal Ministry of Education and Research

Deputy of Research and Technology

Ministry of Health and Medical Education

Islamic Republic of Iran

Publisher

Wiley

Subject

General Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ccr3.574/fullpdf

Reference16 articles.

1. Large deletions and point mutations involving the dedicator of cytokinesis 8 (DOCK8) in the autosomal-recessive form of hyper-IgE syndrome;Engelhardt;J. Allergy Clin. Immunol.,2009

2. Autosomal recessive hyperimmunoglobulin E syndrome: a distinct disease entity;Renner;J. Pediatr.,2004

3. The extended clinical phenotype of 64 patients with dedicator of cytokinesis 8 deficiency;Engelhardt;J. Allergy Clin. Immunol.,2015

4. Combined immunodeficiency associated with DOCK8 mutations;Zhang;N. Engl. J. Med.,2009

5. DOCK8 deficiency;Su;Ann. N. Y. Acad. Sci.,2011

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