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Paper Details

Genetic Variability of Complement Factor H Has Ethnicity-Specific Associations With Choroidal Thickness.
Invest Ophthalmol Vis Sci
2
2023
ARMS2, CETP, CFH, CFH alleles, CFH risk allele rs1061170, CFH variants, CT, Complement Factor H, SFCT, VIPR2, age-related macular degeneration, central serous choroidopathy, genetic alleles, retinal pathology, risk alleles, rs1061170, rs1329428, rs800292
Author NameAffiliation
Youngseok SongSingapore Eye Research Institute
Youngseok SongAsahikawa Medical University
Yih-Chung ThamSingapore Eye Research Institute
Yih-Chung ThamYong Loo Lin School of Medicine, National University of Singapore.
Ching-Yu ChengSingapore Eye Research Institute
Ching-Yu ChengYong Loo Lin School of Medicine, National University of Singapore.
Ching-Yu ChengSingapore Eye Research Institute
Ching-Yu ChengYong Loo Lin School of Medicine, National University of Singapore.
Tien Yin WongTsinghua University
Tien Yin WongTsinghua University
Kelvin Yi Chong Teo
Kelvin Yi Chong TeoSingapore Eye Research Institute
Chui Ming Gemmy Cheung
Chui Ming Gemmy CheungSingapore Eye Research Institute
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