LOXL1 promoter haplotypes are associated with exfoliation syndrome in a u.s. caucasian population

Investigative Ophthalmology and Visual Science

Volumn 52, Issue 5, 2011, Pages 2372-2378

  Fan, Bao Jian ^a   Pasquale, Louis R ^a   Rhee, Douglas ^a   Li, Tiansen ^b   Haines, Jonathan L ^c   Wiggs, Janey L ^a  

^a MASSACHUSETTS EYE AND EAR INFIRMARY   (United States)

^b NATIONAL EYE INSTITUTE   (United States)

^c VANDERBILT UNIVERSITY MEDICAL CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ENZYME; LYSYL OXIDASE LIKE 1; UNCLASSIFIED DRUG;

AGED; ALLELE; ARTICLE; CASE CONTROL STUDY; CAUCASIAN; CONTROLLED STUDY; DISEASE ASSOCIATION; DISEASE PREDISPOSITION; ENZYME ACTIVITY; EXFOLIATION SYNDROME; FEMALE; GENE EXPRESSION; GENETIC RISK; GENETIC TRANSCRIPTION; GENETIC VARIABILITY; GENOTYPE; HAPLOTYPE; HUMAN; MAJOR CLINICAL STUDY; MALE; PRIORITY JOURNAL; PROMOTER REGION; RISK ASSESSMENT; SINGLE NUCLEOTIDE POLYMORPHISM; UNITED STATES;

AGED; AMINO ACID OXIDOREDUCTASES; EUROPEAN CONTINENTAL ANCESTRY GROUP; EXFOLIATION SYNDROME; FEMALE; GLAUCOMA, OPEN-ANGLE; HAPLOTYPES; HUMANS; MALE; POLYMORPHISM, SINGLE NUCLEOTIDE; PROMOTER REGIONS, GENETIC; RISK FACTORS; UNITED STATES;

EID: 79955987576     PISSN: 01460404     EISSN: 15525783     Source Type: Journal    
DOI: 10.1167/iovs.10-6268     Document Type: Article

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