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Functional Characterization of Rare Genetic Variants in the N-Terminus of Complement Factor H in aHUS, C3G, and AMD. (2020)

First Author: Wong EKS

Attributed to: Personalised management of atypical haemolytic uraemic syndrome funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.3389/fimmu.2020.602284

PubMed Identifier: 33519811

Publication URI: http://europepmc.org/abstract/MED/33519811

Type: Journal Article/Review

Volume: 11

Parent Publication: Frontiers in immunology

ISSN: 1664-3224