A common haplotype in the complement regulatory gene factor H (HF1/CFH) predisposes individuals to age-related macular degeneration

Proceedings of the National Academy of Sciences of the United States of America

Volumn 102, Issue 20, 2005, Pages 7227-7232

  Hageman, Gregory S ^a,b   Anderson, Don H ^b   Johnson, Lincoln V ^b   Hancox, Lisa S ^a   Taiber, Andrew J ^a   Hardisty, Lisa I ^a   Hageman, Jill L ^a   Stockman, Heather A ^a   Borchardt, James D ^a   Gehrs, Karen M ^a   Smith, Richard J H ^c   Silvestri, Giuliana ^c   Russell, Stephen R ^a   Klaver, Caroline C W ^d   Barbazetto, Irene ^g   Chang, Stanley ^g   Yannuzzi, Lawrence A ^g   Barile, Gaetano R ^g   Merriam, John C ^g   Smith, R Theodore ^g   Olsh, Adam K ^e   Bergeron, Julie ^f   Zernant, Jana ^g   Merriam, Joanna E ^g   Gold, Bert ^e   Dean, Michael ^e   Allikmets, Rando ^g,h   more..

^a UNIVERSITY OF IOWA   (United States)

^b UNIVERSITY OF CALIFORNIA   (United States)

^c QUEEN'S UNIVERSITY BELFAST   (United Kingdom)

^d ERASMUS UNIVERSITY ROTTERDAM   (Netherlands)

^e NATIONAL CANCER INSTITUTE   (United States)

^f SAIC FREDERICK INC   (United States)

^g Och Spine at New York Presbyterian Hospitals   (United States)

^h NewYork Presbyterian Hospital   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

COMPLEMENT FACTOR H;

ARTICLE; CHROMOSOME 1Q; CHROMOSOME IDENTIFICATION; COHORT ANALYSIS; CONTROLLED STUDY; DISEASE PREDISPOSITION; DRUSEN; GENE FREQUENCY; GENE LOCUS; GENETIC PREDISPOSITION; GENETIC RISK; GENETIC VARIABILITY; HAPLOTYPE; HOMOZYGOTE; HUMAN; HUMAN CELL; LINKAGE ANALYSIS; PIGMENT EPITHELIUM; PRIORITY JOURNAL; PROTEIN SYNTHESIS; RETINA MACULA AGE RELATED DEGENERATION; SIGNAL TRANSDUCTION;

AGED; AGED, 80 AND OVER; COMPLEMENT FACTOR H; DNA MUTATIONAL ANALYSIS; EUROPEAN CONTINENTAL ANCESTRY GROUP; GENE COMPONENTS; GENOTYPE; HAPLOTYPES; HUMANS; IMMUNOHISTOCHEMISTRY; MACULAR DEGENERATION; MIDDLE AGED; MUTATION, MISSENSE; ODDS RATIO; PIGMENT EPITHELIUM OF EYE; POLYMORPHISM, SINGLE NUCLEOTIDE; RISK FACTORS; VARIATION (GENETICS);

EID: 21044453724     PISSN: 00278424     EISSN: None     Source Type: Journal    
DOI: 10.1073/pnas.0501536102     Document Type: Article

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