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frame shift mutation

  • 称码突变

专业释义英英释义

  • 移码突变 - 引用次数：2

    The frame-shift mutation caused by deletion of 540A in GPⅡb gene is a novel mutation which is the genetic defect in the patient with GT.

    GPⅡb基因540A缺失发生移码突变是GPⅡb基因的一种新突变,是血小板无力症发病的分子基础。

    参考来源 - 一种新的GPⅡb基因540A缺失移码突变引起的血小板无力症
  • 移码突变

·2,447,543篇论文数据，部分数据来源于NoteExpress

Frameshift mutation

  • abstract: A frameshift mutation (also called a framing error or a reading frame shift) is a genetic mutation caused by indels (insertions or deletions) of a number of nucleotides in a DNA sequence that is not divisible by three. Due to the triplet nature of gene expression by codons, the insertion or deletion can change the reading frame (the grouping of the codons), resulting in a completely different translation from the original.

以上来源于: WordNet

双语例句

  • Conclusions No functional FANCA protein was found in these 3 cases of FA-A, and intragenic deletion, frame shift and splice site mutation were the major pathogenic mutations found in FANCA gene.

    结论3例FA-A型患者均无功能性FANCA蛋白表达；基因缺失、移码突变和剪切位点突变是FANCA基因的主要失活方式。

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