缺失突变（deletion mutation）是指编码某种氨基酸的密码子经碱基缺失以后，变成编码另一种氨基酸的密码子，从而使多肽链的氨基酸种类和序列发生改变。
... deletion mutant 缺失突变体 deletion mutantion 缺失突变 deletional recombination 缺失重组 ...
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...鞘蛋白22;缺失突变 [gap=1815]to pressure palsies； Autosomal dominant inheritance； Peripheral myelinprotein22； Deletion ...
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... 缺失病征状 deficient symptom 缺失突变 deficiency mutation 缺失异型合子 deletion heterozygote ...
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... modified model 改进的模型 deleted mutagenize 缺失突变 roof bolting 顶板锚杆支护 ...
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结论COL7A1基因的缺失突变和错义突变引起该患者临床症状的特异突变。
The deletion mutation and missense mutation of COL7A1 gene result in the specific mutation in patients with clinical symptoms.
目的制备登革2型病毒中国分离株(DEN2 - 43)的衣壳蛋白缺失突变病毒。
Objective To generate rescued viruses with deletion mutation of capsid protein from dengue virus type 2 isolated in China (DEN2-43).
采用聚合酶链反应（PCR）技术和光密度扫描检测两组线粒体DNA的缺失突变情况。
Deletion mutation state of the two groups of mitochondria DNA were detected by PCR technology and photodensity scan.
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