Insight into the molecular genetics of myopia

Insight into the molecular genetics of myopia
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深入了解近视的分子遗传学

DOI:
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发表时间:
2017-12
期刊:
影响因子:
2.2
通讯作者:
Qingjiong Zhang
Qingjiong Zhang
中科院分区:
医学4区
文献类型:
--
作者:
Jiali Li;Qingjiong Zhang

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近视是全世界最常见的视力损害原因。遗传和环境因素会导致近视的发生。近视的分子遗传学研究已经建立,并暗示了遗传因素的重要作用。通过连锁分析、关联研究、测序分析和实验性近视研究,已经确定了许多与近视相关的位点和基因。迄今为止,还没有基于不同的方法对非综合征性和综合征性近视相关的位点和基因进行系统的综述。这种对近视分子遗传学的系统回顾将为识别其他可能的近视基因提供线索,并帮助我们了解近视的分子机制。本文综述了近年来近视的遗传学研究,总结了所有可能报道的与近视相关的基因和位点,并对未来近视分子遗传学的研究提出了建议。
Myopia is the most common cause of visual impairment worldwide. Genetic and environmental factors contribute to the development of myopia. Studies on the molecular genetics of myopia are well established and have implicated the important role of genetic factors. With linkage analysis, association studies, sequencing analysis, and experimental myopia studies, many of the loci and genes associated with myopia have been identified. Thus far, there has been no systemic review of the loci and genes related to non-syndromic and syndromic myopia based on the different approaches. Such a systemic review of the molecular genetics of myopia will provide clues to identify additional plausible genes for myopia and help us to understand the molecular mechanisms underlying myopia. This paper reviews recent genetic studies on myopia, summarizes all possible reported genes and loci related to myopia, and suggests implications for future studies on the molecular genetics of myopia.
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