Whole-exome sequencing identifies rare, functional CFH variants in families with macular degeneration. (2014)
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/10.1093/hmg/ddu226
PubMed Identifier: 24847005
Publication URI: http://europepmc.org/abstract/MED/24847005
Type: Journal Article/Review
Volume: 23
Parent Publication: Human molecular genetics
Issue: 19
ISSN: 0964-6906