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儿童脊髓性肌萎缩症的基因诊断研究进展 被引量:4

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摘要 儿童脊髓性肌萎缩症居致死性常染色体隐性遗传病的第二位。近年来,该病的致病基因被定位于5q13,目前发现与该病有关的基因有运动神经元存活基因、神经元凋亡抑制蛋白基因、基本转录因子2p44基因。本文对该病的最新基因学及基因诊断学进展做一综述。
出处 《国外医学(遗传学分册)》 2005年第5期281-284,共4页 Foreign Medical Sciences(Section of Genetics )
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同被引文献49

  • 1杨元,彭茜,阿周存,林立.运用DHPLC技术进行脊髓性肌萎缩症SMN-T基因缺失检测的初步研究[J].临床儿科杂志,2005,23(5):271-274. 被引量:3
  • 2陈万金,吴志英,王柠,林珉婷,慕容慎行.脊髓性肌萎缩症运动神经元生存基因2拷贝数与临床表型的关系[J].中华神经科杂志,2005,38(11):673-676. 被引量:11
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