Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
8952438 | Ophthalmology | 2018 | 11 Pages |
Abstract
This study supported a role for protein-altering variants in the COL8A1 gene in AMD pathogenesis. We demonstrated the presence of Col8a1 in Bruch's membrane, further supporting the role of COL8A1 variants in AMD pathogenesis. Protein-altering variants in COL8A1 may alter the integrity of Bruch's membrane, contributing to the accumulation of drusen and the development of AMD.
Keywords
CNVNC2NC1TIMP3CADDGATKCFHARMS2WESCFIAMDPBSMAFSIFTCMCChoroidal neovascularizationgeographic atrophyGenome Analysis ToolkitCombined Annotation Dependent DepletionWhole-exome sequencingComplement factor Hage-related maculopathy susceptibility 2Complement Factor Iminor allele frequencyPhosphate-buffered salineGenome-wide association studyGWASSingle nucleotide polymorphismSNP
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Authors
Jordi PhD, Johanna M. MD, MSc, Maartje J. PhD, Marc MSc, Bjorn BSc, Najaf PhD, Laura MSc, Eveline MD, MSc, Alejandro PhD, Joost A.M. MSc, Jeroen G.J. BSc, Robert PhD, Paulus T.V.M. MD, PhD, Albert MD, PhD, Johannes R. MD, PhD, Tina MD, Sascha MD, PhD,