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常染色体显性视网膜色素变性的相关基因研究进展 被引量:6

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摘要 常染色体显性视网膜色素变性 (autosomal dominant retinitis pigmentosa,ad RP)属视网膜色素变性的一种类型 ,是单基因遗传病 ,具有遗传异质性和临床异质性。目前已克隆了 8个致病基因 ,包括 RHO、Peripherin/ RDS、RP1、NRL、CRX等 ,现简介如下。
作者 邓新国
出处 《国外医学(遗传学分册)》 2002年第3期173-177,共5页 Foreign Medical Sciences(Section of Genetics )
基金 美国 CMB资金资助 (No.98-677)
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参考文献40

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共引文献5

同被引文献81

  • 1庄文娟,盛迅伦.常染色体显性遗传视网膜色素变性的相关基因研究概况[J].国际眼科杂志,2004,4(5):868-872. 被引量:9
  • 2Xiao-liZhang,MingLiu,Xiao-hongMeng,Wei-lingFu,Zheng-qinYin,XueZhang,Jun-fuHuang.A COMPLETE SCREEN FOR MUTATIONS OF THE RHODOPSIN GENE IN A PANEL OF CHINESE PATIENTS WITH AUTOSOMAL DOMINANT RETINITIS PIGMENTOSA[J].Chinese Medical Sciences Journal,2005,20(1):30-34. 被引量:7
  • 3张馨方,盛迅伦.视网膜色素变性的相关基因研究进展[J].国际眼科杂志,2006,6(3):654-657. 被引量:10
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