Associations of polymorphisms in LOXL1 and copper chaperone genes with pseudoexfoliation-syndrome-related cataract in a Chinese Uygur population.

Qinghe JingDan LiWei GaoFan ZhangYi LuYong-Xiang Jiang

Published in: International ophthalmology (2020)

The rs3825942 SNP of LOXL1 was strongly associated with PEXC in this Uygur population in China. CCS variants may represent a risk factor for PEXC. Our findings expand the understanding of the genetic base of PEXC.

Keyphrases

genome wide
copy number
dna methylation
gene expression
endoplasmic reticulum
genetic diversity
genome wide identification