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原发性开角型青光眼的相关基因研究进展

艾力江·艾尔肯 具尔提·哈第尔

国际眼科杂志Issue(4):651-653,3.
国际眼科杂志Issue(4):651-653,3.DOI:10.3980/j.issn.1672-5123.2014.04.20

原发性开角型青光眼的相关基因研究进展

Research progress on related genes for primary open angle glaucoma

艾力江·艾尔肯 1具尔提·哈第尔1

作者信息

  • 1. 830054 中国新疆维吾尔自治区乌鲁木齐市,新疆医科大学第一附属医院眼科
  • 折叠

摘要

Abstract

Primary open angle glaucoma ( POAG ) is the main cause of blindness with visual field damage and optic nerve degeneration.In recent years, a lot of researches have been done, showing that genetic factors and gene mutation play an important role in POAG.There are more than 20 related POAG genes. Now we will review the related genes of POAG, especially the well known causative genes of MYOC, OPTN, WDR36, and CAV1/CAV2, in terms of their locations, structures, research progress, et al, and provide a reference for genetic research in primary open-angle glaucoma.

关键词

原发性开角型青光眼/基因变异/遗传/研究进展

Key words

primary open angle glaucoma/gene mutation/heredity/research progress

引用本文复制引用

艾力江·艾尔肯,具尔提·哈第尔..原发性开角型青光眼的相关基因研究进展[J].国际眼科杂志,2014,(4):651-653,3.

国际眼科杂志

OACSTPCD

1672-5123

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