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Statistical Validation of Rare Complement Variants Provides Insights into the Molecular Basis of Atypical Hemolytic Uremic Syndrome and C3 Glomerulopathy. (2018)

First Author: Osborne AJ

Attributed to: Unravelling the mechanism of complement activation via the lectin pathway funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.4049/jimmunol.1701695

PubMed Identifier: 29500241

Publication URI: http://europepmc.org/abstract/MED/29500241

Type: Journal Article/Review

Volume: 200

Parent Publication: Journal of immunology (Baltimore, Md. : 1950)

Issue: 7

ISSN: 0022-1767