Risk Alleles Associated with Neovascularization in a Pachychoroid Phenotype

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Veröffentlicht in:	Ophthalmology (Rochester, Minn.) Minn.), 2016-12, Vol.123 (12), p.2628-2630
Hauptverfasser:	Dansingani, Kunal K., MA, FRCOphth, Perlee, Lorah T., PhD, Hamon, Sara, PhD, Lee, May, MST, Shah, Vinnie P., MD, Spaide, Richard F., MD, Sorenson, John, MD, Klancnik, James M., MD, Yannuzzi, Lawrence A., MD, Barbazetto, Irene A., MD, Cooney, Michael J., MD, MBA, Engelbert, Michael, MD, PhD, Chen, Christine, PhD, FRANZCO, Hewitt, Alex W., PhD, FRANZCO, Freund, K. Bailey, MD
Format:	Artikel
Sprache:	eng
Schlagworte:	Aged Aged, 80 and over Apolipoproteins - genetics Case-Control Studies Choroid Diseases - diagnosis Choroid Diseases - genetics Choroidal Neovascularization - diagnosis Choroidal Neovascularization - genetics Complement C2 Complement C3 - genetics Complement Factor B - genetics Complement Factor H - genetics Complement System Proteins - genetics Eye Proteins - genetics Factor XIII - genetics Female Gene Frequency Humans Male Middle Aged Ophthalmology Phenotype Polymorphism, Single Nucleotide Proteins - genetics Risk Factors Wet Macular Degeneration - diagnosis Wet Macular Degeneration - genetics
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