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采用9对引物检测假肥大型肌营养不良症的基因缺失
引用本文:赵振军,叶贤坤,张义芳,王小会,牛丽霞. 采用9对引物检测假肥大型肌营养不良症的基因缺失[J]. 河北医药, 2001, 23(2): 98-99
作者姓名:赵振军  叶贤坤  张义芳  王小会  牛丽霞
作者单位:050091,石家庄,河北以岭医药研究院
摘    要:目的:研究快速、准确检测假肥大型肌营养不良(DMD/BMD)基因缺失的方法。方法:采用9对引物的多重链式聚合酶反应(mPCR)检测169例DMD/BMD基因缺失。结果:169例患者中85例检测出基因缺失,总缺失率为50.3%。结论:9对引物的mPCR在DMD/BMD基因缺失诊断中具有快速、准确、经济、实用等特点,便于推广。

关 键 词:肌营养不良 基因缺失 mPCR 假肥大型肌营养不良反应 引物检测
修稿时间:2000-08-10

Detection of muscular dystrophy gene deletions by 9 pairs of primers
ZHAO Zhenjun,YE Xiankun,ZHANG Yifang,et al.. Detection of muscular dystrophy gene deletions by 9 pairs of primers[J]. Hebei Medical Journal, 2001, 23(2): 98-99
Authors:ZHAO Zhenjun  YE Xiankun  ZHANG Yifang  et al.
Affiliation:ZHAO Zhenjun,YE Xiankun,ZHANG Yifang,et al.He Bei Yiling Medical Research Institute,Shijiazhuang 050091
Abstract:Objective To investigate a quick and accurate method in detection of DMD/BMD gene deletions.Methods Detection of DMD/BMD gene deletions by mPCR of 9 pairs of primers was applied.Results 85 patients' gene was deleted in 169.The total rate of deletions was 50.3%.Conclusion mPCR of 9 pairs of primers was a quick accurate economic and practical method in detection of DMD/BMD gene deletions.
Keywords:muscular dystrophy  gene deletion  mPCR
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