AUTHOR=Zhao Fuxin , Chen Wei , Zhou Hui , Reinach Peter S. , Wang Yuhan , Juo Suh-Hang H. , Yang Zhenglin , Xue Anquan , Shi Yi , Liang Chung-Ling , Zeng Changqing , Qu Jia , Zhou Xiangtian TITLE=PDE4B Proposed as a High Myopia Susceptibility Gene in Chinese Population JOURNAL=Frontiers in Genetics VOLUME=12 YEAR=2022 URL=https://www.frontiersin.org/journals/genetics/articles/10.3389/fgene.2021.775797 DOI=10.3389/fgene.2021.775797 ISSN=1664-8021 ABSTRACT=
Myopia is the most common cause of refractive error worldwide. High myopia is a severe type of myopia, which usually accompanies pathological changes in the fundus. To identify high myopia susceptibility genes, DNA-pooling based genome-wide association analysis was used to search for a correlation between single nucleotide polymorphisms and high myopia in a Han Chinese cohort (cases vs. controls in discovery stage: 507 vs. 294; replication stage 1: 991 vs. 1,025; replication stage 2: 1,021 vs. 52,708). Three variants (rs10889602T/G, rs2193015T/C, rs9676191A/C) were identified as being significantly associated with high myopia in the discovery, and replication stage. rs10889602T/G is located at the third intron of phosphodiesterase 4B (