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作 者:杜传书[1,2] 任晓琴[1,2] 江悦华 陈路明[1,2] 蒋玮莹[1,2]
机构地区:[1]中山医科大学医学遗传学研究室 [2]广州军区广州总医院
出 处:《中华血液学杂志》1999年第4期191-193,共3页Chinese Journal of Hematology
基 金:国家自然科学基金
摘 要:目的应用突变特异性扩增系统(ARMS)法筛查广东省常见的葡萄糖6磷酸脱氢酶(G6PD)基因的G1388A、G1376T和A95G,并初步估计其频率。方法应用已建立的G1388A和G1376TARMS法和新建立的A95GARMS法,对90例广东地区男性,经G6PD定性和定量证明为G6PD缺乏者进行检测。结果在90例男性中检出G1388A42例(467%),G1376T14例(156%),A95G12例(133%),共计72例(756%)。其余为稀有突变和未定型者。结论ARMS法为一种简便、快速、经济、准确的检测G6PD基因常见突变的方法。Objective To detect three common G6PD gene point mutations,G1388A,G1376T and A95G,in Guangdong province and to estimate the approximate frequencies.Methods Using the amplification refractory mutation system(ARMS) method to detect G1388A and G1376T and the newly developed ARMS to identify A95G mutation.Results Ninety cases of G6PD deficient male were examined,and 42 of them were identified to be G1388A(46 7 %),14 G1376T(15 6%),and 12 A95G(13 3%). Totally 68 out of the 90 cases(75 6%) were of the three common mutations.The rest belong to rare or undefined mutations.Conclusion ARMS method can be used in detecting common mutations of G6PD gene with the benefits of simple,fast,economic,and accurate.
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