P67-phox (NCF2) Lacking Exons 11 and 12 Is Functionally Active and Leads to an Extremely Late Diagnosis of Chronic Granulomatous Disease (CGD)-Reference-Cited by-同舟云学术

P67-phox (NCF2) Lacking Exons 11 and 12 Is Functionally Active and Leads to an Extremely Late Diagnosis of Chronic Granulomatous Disease (CGD)

Published:2012-04-13 Issue:4 Volume:7 Page:e34296
ISSN:1932-6203
Container-title:PLoS ONE
language:en
Short-container-title:PLoS ONE

Author:

Roesler Joachim,Segerer Florian,Morbach Henner,Kleinert Stefan,Thieme Sebastian,Rösen-Wolff Angela,Liese Johannes G.

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

Reference33 articles.

1. Successful unrelated bone marrow transplantation in a child with chronic granulomatous disease complicated by pulmonary and cerebral granuloma formation.;C Schuetz;Eur J Pediatr,2006

2. Genetic, biochemical, and clinical features of chronic granulomatous disease.;BH Segal;Medicine (Baltimore),2000

3. Chronic granulomatous disease: the European experience.;JM van den Berg;PLoS One,2009

4. Chronic granulomatous disease. Report on a national registry of 368 patients.;JA Winkelstein;Medicine (Baltimore),2000

5. Long-term follow-up and outcome of 39 patients with chronic granulomatous disease.;J Liese;J Pediatr,2000

Cited by 9 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Clinical presentation, diagnosis, and treatment of chronic granulomatous disease;Frontiers in Pediatrics;2024-06-28

2. Hematologically important mutations: The autosomal forms of chronic granulomatous disease (third update);Blood Cells, Molecules, and Diseases;2021-12

3. A novel variant in the neutrophil cytosolic factor 2 (NCF2) gene results in severe disseminated BCG infectious disease: A clinical report and literature review;Molecular Genetics & Genomic Medicine;2020-04-12

4. Human CD40 ligand deficiency dysregulates the macrophage transcriptome causing functional defects that are improved by exogenous IFN-γ;Journal of Allergy and Clinical Immunology;2017-03

5. Genetic disorders coupled to ROS deficiency;Redox Biology;2015-12