{"id":"W2125236492","doi":"10.1073/pnas.0501536102","title":"A common haplotype in the complement regulatory gene factor H ( <i>HF1/CFH</i> ) predisposes individuals to age-related macular degeneration","year":2005,"lang":"en","type":"article","venue":"Proceedings of the National Academy of Sciences","topic":"Retinal Diseases and Treatments","field":"Medicine","cited_by":1968,"is_retracted":false,"has_abstract":true,"ca_institutions":"","funders":"National Eye Institute; National Cancer Institute; U.S. Department of Health and Human Services; National Institutes of Health; Queen's University; Retina Research Foundation; Research to Prevent Blindness","keywords":"Haplotype; Macular degeneration; Factor H; Drusen; Biology; Single-nucleotide polymorphism; Genetics; Locus (genetics); Odds ratio; Complement factor B; Allele; Genotype; Gene; Complement system; Medicine; Pathology; Antibody; Ophthalmology","routes":{"ca_aff":false,"ca_fund":true,"ca_venue":false,"about_ca":false,"invisible_to_affiliation_only":true},"retraction":null,"screen":null}