A missense mutation(G1010A) in exon 3 of HR was also identified in the
患者弟弟的HR基因的第3外显子也存在G1010A的错义突变。
参考来源 - 伴丘疹性损害先天性无毛症家系无毛基因突变的研究·2,447,543篇论文数据,部分数据来源于NoteExpress
以上来源于: WordNet
Missense mutation a point mutation that causes a change in one amino acid of a protein.
错义突变引起蛋白质中一个氨基酸变化的点突变。
DNA damage caused by many factors may lead to missense mutation, deletion or illegal recombination.
多种因素可以引起DNA损伤而最终导致基因产生错义突变、缺失或错误重组。
Missense mutation — a mutation that changes a codon specific for one amino acid to specify another amino acid.
突变成编码另一种氨基酸的密码子。
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