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应用Amp-FLP单体型连锁分析检测Wilson''s患者的基因突变
引用本文:陈悦,佟彤,高文英,宋力,乔丽津. 应用Amp-FLP单体型连锁分析检测Wilson''s患者的基因突变[J]. 天津医药, 2003, 31(11): 704-706
作者姓名:陈悦  佟彤  高文英  宋力  乔丽津
作者单位:300074,天津市儿童医院
摘    要:目的:探讨STR位点变异基因型诊断Wilson’s疾病(wD)的价值。方法:采用Amp—FLP分析方法检测了4个WD患儿及其家系3个位点的基因型。结果:4例先证者均为纯合子,14例家系成员中1例为WD患者,10例为WD基因携带者,2例为正常人,另有1例推断为WD基因携带者。结论:用连锁分析方法检测STR位点,确定相关个体的基因型,方法简便、灵敏、可靠。

关 键 词:Amp-FLP 检测 Wilson’s 基因突变 肝豆状核变性 扩增片段长度多态性 STR位点 单体型连锁分析

Detection of Gene Mutation in Patients with Wilson''s disease by Amplified Fragment Length Polymorphism Analysis
CHEN Yue,TONG Tong,GAO Wenying,SONG Li,QIAO LijinTianjin Children's Hospital,Tianjin ,China. Detection of Gene Mutation in Patients with Wilson''s disease by Amplified Fragment Length Polymorphism Analysis[J]. Tianjin Medical Journal, 2003, 31(11): 704-706
Authors:CHEN Yue  TONG Tong  GAO Wenying  SONG Li  QIAO LijinTianjin Children's Hospital  Tianjin   China
Affiliation:CHEN Yue,TONG Tong,GAO Wenying,SONG Li,QIAO LijinTianjin Children's Hospital,Tianjin 300074,China
Abstract:Objective:To detect the gene mutation in patients with Wilson's disease(WD)by amplified fragment length polymorphism(Amp-FLP)analysis.Methods:The genotypes of 3 STRsites were detected by Amp-FLP in 4 children with WD and their families.Results:The 4 probands were of homozygote.their families(n=14)were patients with WD(n=1),WD gene-carriers(n=10),normal persons(n=2)and predicted WD gene-carriers(n=1).Conclusion:In order to identify the relative genotype,the detection of STRsite by Amp-FLP is a simple,accurate and feasible method.
Keywords:hepatolenticular degeneration polymorphism  restriction fragment length genes mutation
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