Classical and Non-classical Presentations of Complement Factor I Deficiency: Two Contrasting Cases Diagnosed via Genetic and Genomic Methods-Reference-Cited by-同舟云学术

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Classical and Non-classical Presentations of Complement Factor I Deficiency: Two Contrasting Cases Diagnosed via Genetic and Genomic Methods

Published:2019-06-07 Issue: Volume:10 Page:
ISSN:1664-3224
Container-title:Frontiers in Immunology
language:
Short-container-title:Front. Immunol.

Author:

Shields Adrian M.,Pagnamenta Alistair T.,Pollard Andrew J.,Taylor Jenny C.,Allroggen Holger,Patel Smita Y.,

Funder

Wellcome Trust

National Institute for Health Research

Publisher

Frontiers Media SA

Subject

Immunology,Immunology and Allergy

Reference31 articles.

1. Processing of human factor I in COS-1 cells co-transfected with factor I and paired basic amino acid cleaving enzyme (PACE) cDNA;Wong;Mol Immunol.,1995

2. Regulator-dependent mechanisms of C3b processing by factor I allow differentiation of immune responses;Xue;Nat Struct Mol Biol.,2017

3. Invasive pneumococcal disease in children can reveal a primary immunodeficiency;Gaschignard;Clin Infect Dis. (

4. Novel CFI mutation in a patient with leukocytoclastic vasculitis may redefine the clinical spectrum of Complement Factor I deficiency;Bay;Clin Immunol.,2015

5. Molecular characterization of two novel cases of complete complement inhibitor Factor I deficiency;Nita;Mol Immunol.,2011

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