Functional Characterization of Rare Genetic Variants in the N-Terminus of Complement Factor H in aHUS, C3G, and AMD. (2020)
Attributed to:
Genetic and Acquired Complement Abnormalities in Idiopathic Membranoproliferative Glomerulonephritis
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