C-reactive protein and CFH, ARMS2/HTRA1 gene variants are independently associated with risk of macular degeneration

Ophthalmology

Volumn 117, Issue 8, 2010, Pages 1560-1566

  Seddon, Johanna M ^a   Gensler, Gary ^b   Rosner, Bernard ^c  

^a TUFTS UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b EMMES CORPORATION   (United States)

^c HARVARD MEDICAL SCHOOL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

C REACTIVE PROTEIN; COMPLEMENT FACTOR H;

AGED; ARMS2 GENE; ARTICLE; BODY MASS; CASE CONTROL STUDY; CFH GENE; CONFIDENCE INTERVAL; DRUSEN; EDUCATION; FEMALE; GENE; GENETIC ANALYSIS; GENETIC VARIABILITY; GENOTYPE; HTRA1 GENE; HUMAN; LOGISTIC REGRESSION ANALYSIS; MAJOR CLINICAL STUDY; MALE; OUTCOME ASSESSMENT; PRIORITY JOURNAL; PROTEIN BLOOD LEVEL; RETINA MACULA DEGENERATION; RETINA MACULOPATHY; RETINA NEOVASCULARIZATION; RISK FACTOR; SINGLE NUCLEOTIDE POLYMORPHISM; SMOKING; VITAMIN SUPPLEMENTATION;

AGED; C-REACTIVE PROTEIN; CASE-CONTROL STUDIES; COMPLEMENT FACTOR H; FEMALE; GENOTYPE; GEOGRAPHIC ATROPHY; HUMANS; MACULAR DEGENERATION; MALE; POLYMORPHISM, SINGLE NUCLEOTIDE; PROTEINS; QUESTIONNAIRES; RETINAL DRUSEN; RISK FACTORS; SERINE ENDOPEPTIDASES;

EID: 77955473846     PISSN: 01616420     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ophtha.2009.11.020     Document Type: Article

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