Strong association of the Y402H variant in complement factor H at 1q32 with susceptibility to age-related macular degeneration

American Journal of Human Genetics

Volumn 77, Issue 1, 2005, Pages 149-153

  Zareparsi, Sepideh ^a   Branham, Kari E H ^a   Li, Mingyao ^b   Shah, Sapna ^a   Klein, Robert J ^c   Ott, Jurg ^c   Hoh, Josephine ^d   Abecasis, Goņalo R ^b   Swaroop, Anand ^a,e  

^a UNIVERSITY OF MICHIGAN MEDICAL SCHOOL   (United States)

^b UNIVERSITY OF MICHIGAN   (United States)

^c ROCKEFELLER UNIVERSITY   (United States)

^d YALE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^e UNIVERSITY OF MICHIGAN   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

APOLIPOPROTEIN E; COMPLEMENT FACTOR H; TOLL LIKE RECEPTOR 4;

ADULT; AGED; AMINO ACID SUBSTITUTION; ARTICLE; BLINDNESS; CASE CONTROL STUDY; CHROMOSOME 1Q; CONTROLLED STUDY; ETHNOLOGY; FAMILY HISTORY; FEMALE; GENE DOSAGE; GENE FREQUENCY; GENETIC SUSCEPTIBILITY; GENETIC VARIABILITY; GENOTYPE; HOMOZYGOTE; HUMAN; INNATE IMMUNITY; MAJOR CLINICAL STUDY; MALE; PREVALENCE; PRIORITY JOURNAL; RETINA MACULA AGE RELATED DEGENERATION; STATISTICAL ANALYSIS; SUBRETINAL NEOVASCULARIZATION;

EID: 20544471911     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/431426     Document Type: Article

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