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Mutational screening of AGRN, SLC39A5, SCO2, P4HA2, BSG, ZNF644, and CPSF1 in a Chinese cohort of 103 patients with nonsyndromic high myopia.

Molecular vision - 1 Jan 2021

Zheng Yi-Han, Cai Xue-Bi, Xia Lu-Qi, Zhou Fang-Yue, Wen Xin-Ran, Chen De-Fu, Han Fang, Zhou Kai-Jing, Jin Zi-Bing, Zhuang Wen-Juan, Lin Bing

Abstract excerpt

Purpose: High myopia (HM) is one of the leading causes of irreversible vision loss in the world. Many myopia loci have been uncovered with linkage analysis, genome-wide association studies, and sequencing analysis. Numerous pathogenic genes within these loci have been detected in a portion of HM cases. In the present study, we aimed to investigate the genetic basis of 103 patients with nonsyndromic HM, focusing...

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PMID: 35002215
PMCID: PMC8684808

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

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