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