儿童发展性阅读障碍遗传基因的相关研究

中国儿童保健杂志 ›› 2011, Vol. 19 ›› Issue (3): 236-239.

儿童发展性阅读障碍遗传基因的相关研究

左彭湘^1,2,吴汉荣¹,李增春²

1 华中科技大学同济医学院儿少卫生与妇幼保健系,湖北武汉 430030;
2 石河子大学医学院,新疆石河子 832002

收稿日期:2011-01-04 发布日期:2011-03-06 出版日期:2011-03-06
通讯作者: 吴汉荣, E-mail:wuhr0522@163.com
作者简介:左彭湘(1975-), 女,湖南人,主要研究方向为儿童青少年心理卫生
基金资助:
国家自然科学基金(30872132)

Received:2011-01-04 Online:2011-03-06 Published:2011-03-06

摘要/Abstract

摘要： 对汉族儿童阅读障碍的发病机制从遗传学角度进行探索,旨在了解汉族儿童发展性阅读障碍的遗传候选基因研究策略与未来的研究的方向,文章从发展性阅读障碍遗传候选基因的发现的研究进程进行归纳与综述,探讨了相关基因的发现与功能。得出DCDC2,KIAA0319和DYX1C1是发展性阅读障碍的候选基因,功能研究的表明,他们都参与了大脑发育过程中神经元迁移的作用,对它们的进行更进一步的研究将成为未来的研究方向

中图分类号:

R749.94

左彭湘,吴汉荣,李增春. 儿童发展性阅读障碍遗传基因的相关研究[J]. 中国儿童保健杂志, 2011, 19(3): 236-239.

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