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Whole-exome sequencing identifies rare, functional CFH variants in families with macular degeneration (2014)

First Author: Yu Y

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

Parent Publication: Human Molecular Genetics

Issue: 19

ISSN: 0964-6906