Genetic variants in complement pathway and ARMS2/HTRA1 genes and risk of age-related macular degeneration in a homogeneous population from central Greece
dc.creator | Tsiloulis A.N., Zacharaki F., Kotoula M.G., Chatzoulis D.Z., Morrison M.A., Mayne K., Dardiotis E., Stefanidis I.L., Almpanidou P., DeAngelis M.M., Tsironi E.E. | en |
dc.date.accessioned | 2023-01-31T10:14:27Z | |
dc.date.available | 2023-01-31T10:14:27Z | |
dc.date.issued | 2016 | |
dc.identifier | 10.3109/13816810.2015.1045525 | |
dc.identifier.issn | 13816810 | |
dc.identifier.uri | http://hdl.handle.net/11615/79974 | |
dc.description.abstract | [No abstract available] | en |
dc.language.iso | en | en |
dc.source | Ophthalmic Genetics | en |
dc.source.uri | https://www.scopus.com/inward/record.uri?eid=2-s2.0-84958554293&doi=10.3109%2f13816810.2015.1045525&partnerID=40&md5=19c1d65926e70b6785582eec04c0c2d6 | |
dc.subject | age related maculopathy susceptibility 2 protein | en |
dc.subject | complement factor H | en |
dc.subject | high temperature requirement factor A1 | en |
dc.subject | protein | en |
dc.subject | unclassified drug | en |
dc.subject | ARMS2 protein, human | en |
dc.subject | complement | en |
dc.subject | HtrA1 protein, human | en |
dc.subject | protein | en |
dc.subject | serine protease HTRA1 | en |
dc.subject | age related macular degeneration | en |
dc.subject | aged | en |
dc.subject | allele | en |
dc.subject | chromosome 10 | en |
dc.subject | cohort analysis | en |
dc.subject | controlled study | en |
dc.subject | eye examination | en |
dc.subject | female | en |
dc.subject | fluorescence angiography | en |
dc.subject | gene linkage disequilibrium | en |
dc.subject | genetic association | en |
dc.subject | genetic variability | en |
dc.subject | genotype | en |
dc.subject | geographic atrophy | en |
dc.subject | Greece | en |
dc.subject | human | en |
dc.subject | Letter | en |
dc.subject | major clinical study | en |
dc.subject | male | en |
dc.subject | optical coherence tomography | en |
dc.subject | priority journal | en |
dc.subject | single nucleotide polymorphism | en |
dc.subject | subretinal neovascularization | en |
dc.subject | wet macular degeneration | en |
dc.subject | Caucasian | en |
dc.subject | epidemiology | en |
dc.subject | genetics | en |
dc.subject | genotyping technique | en |
dc.subject | geographic atrophy | en |
dc.subject | risk factor | en |
dc.subject | wet macular degeneration | en |
dc.subject | Aged | en |
dc.subject | Complement System Proteins | en |
dc.subject | European Continental Ancestry Group | en |
dc.subject | Female | en |
dc.subject | Genotyping Techniques | en |
dc.subject | Geographic Atrophy | en |
dc.subject | Greece | en |
dc.subject | High-Temperature Requirement A Serine Peptidase 1 | en |
dc.subject | Humans | en |
dc.subject | Linkage Disequilibrium | en |
dc.subject | Male | en |
dc.subject | Polymorphism, Single Nucleotide | en |
dc.subject | Proteins | en |
dc.subject | Risk Factors | en |
dc.subject | Wet Macular Degeneration | en |
dc.subject | Taylor and Francis Ltd | en |
dc.title | Genetic variants in complement pathway and ARMS2/HTRA1 genes and risk of age-related macular degeneration in a homogeneous population from central Greece | en |
dc.type | other | en |
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