移码突变(frameshift mutation ) :在正常的DNA 分子中,碱基缺失或增加非3的倍数,造成这位置之后的一系列编码发生移位错误的改变,这种现象称移码突变。
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frameshift mutation(框移突变): a mutation of insertion or deletion of a genetic material that leads to a shift in the translation of the reading fra...
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reading frameshift mutation 读框移码突变
Frameshift mutation frequency 移码突变率
suppressible frameshift mutation 可抑制移码突变
Because cd53 (-T) results in a 59 amino acidsβglobin variant, it is the first frameshift mutation reported in exon 2 leading to a truncatedβ-globin variant and producing dominantly inheritedβthalassemia.
由于cd53(-T)导致含有59个氨基酸的β珠蛋白变异体,所以这是第一个位于第二外显子上的导致截短的β珠蛋白变异体并引起显性遗传性β地贫的移码突变。
参考来源 - 一种见于苗族家系的导致显性遗传性β地中海贫血的新移码突变的鉴定·2,447,543篇论文数据,部分数据来源于NoteExpress
以上来源于: WordNet
The mutations in patients with factor V deficiency were identified including point mutation, frameshift mutation, deletion and insertion mutation.
本课题在对具有先天性出血倾向的门诊患者进行筛查的过程中,发现了一例重型凝血因子V缺乏症患者。
We show that sodium channels with the missense mutation recover from inactivation more rapidly than normal and that the frameshift mutation causes the sodium channel to be non-functional.
电生理研究显示含有错义突变的钠离子通道比正常通道从静止中恢复的更快,而读码突变使钠离子通道失去功能。
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