Common variants in the complement factor H gene confer genetic susceptibility to central serous chorioretinopathy

Ophthalmology

Volumn 121, Issue 5, 2014, Pages 1067-1072

  Miki, Akiko ^a   Kondo, Naoshi ^a,b   Yanagisawa, Suiho ^a   Bessho, Hiroaki ^a   Honda, Shigeru ^a   Negi, Akira ^a  

^a KOBE UNIVERSITY GRADUATE SCHOOL OF MEDICINE   (Japan)

^b Medical Corporation Ryokuwakai Kondo Ophthalmic Clinic   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

COMPLEMENT FACTOR H;

ADULT; ARTICLE; CENTRAL SEROUS RETINOPATHY; CONTROLLED STUDY; CROSS-SECTIONAL STUDY; DISEASE ASSOCIATION; FEMALE; GENE FREQUENCY; GENETIC ASSOCIATION; GENETIC MODEL; GENETIC SUSCEPTIBILITY; GENETIC VARIABILITY; GENOTYPE; HAPLOTYPE; HEREDITY; HUMAN; MAJOR CLINICAL STUDY; MALE; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM;

ADULT; AGED; AGED, 80 AND OVER; CASE-CONTROL STUDIES; CENTRAL SEROUS CHORIORETINOPATHY; COMPLEMENT FACTOR H; CROSS-SECTIONAL STUDIES; FEMALE; GENE FREQUENCY; GENETIC PREDISPOSITION TO DISEASE; GENOTYPE; GENOTYPING TECHNIQUES; HUMANS; MALE; MIDDLE AGED; POLYMERASE CHAIN REACTION; POLYMORPHISM, SINGLE NUCLEOTIDE;

EID: 84899948846     PISSN: 01616420     EISSN: 15494713     Source Type: Journal    
DOI: 10.1016/j.ophtha.2013.11.020     Document Type: Article

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