Novel pathogenic mutations identified in the first Chinese pedigree of complete C6 deficiency
Author:
Affiliation:
1. Division of Rheumatology & Clinical Immunology Department of Medicine Queen Mary Hospital The University of Hong Kong Hong Kong
2. Division of Clinical Immunology Department of Pathology Queen Mary Hospital Hong Kong
Publisher
Wiley
Subject
General Nursing,Immunology,Immunology and Allergy
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/cti2.1148
Reference29 articles.
1. European Society for Immunodeficiencies (ESID) and European Reference Network on Rare Primary Immunodeficiency, Autoinflammatory and Autoimmune Diseases (ERN RITA) Complement Guideline: Deficiencies, Diagnosis, and Management
2. Properties of a low molecular weight complement component C6 found in human subjects with subtotal C6 deficiency;Orren A;Immunology,1992
3. Complement deficiencies and dysregulation: Pathophysiological consequences, modern analysis, and clinical management
4. Human genetics of meningococcal infections
5. Clinical and Genetic Spectrum of a Large Cohort With Total and Sub-total Complement Deficiencies
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