nonsense mutation

Identification of a nonsense mutation causing X-linked RP 2 in two Chinese families

两个家系中X连锁视网膜色素变性的RP2基因无义突变

Case had 1 base pair insertion TT → TAT in 85 codon and 1 base pair deletion GCA → GA, which may result in nonsense mutation.

1例85密码子第2、3碱基之间插入A，同时86密码子第2碱基缺失，即GCA→GA导致无义突变。

The nature of all the three mutant alleles of this group is nonsense mutation disrupting the coding region of oxt gene.

该组的三个突变体等位基因的突变都是无义突变，它们都破坏了。Xt基因的编码区。

Gonadial Abnormality and Homozygous Decease from the Nonsense Mutation of Kit in W~ (-3Bao) Mouse

Kit无义突变致W~（-3Bao）小鼠生殖腺异常及纯合子贫血死亡

There was a wide spectrum of mutation type including frame shift, nonsense, splice site mutation, in frame insertion or deletion and missense mutations.

突变类型包括移码突变、无义突变、剪接异常、框架内插入或缺失以及错义突变。

Hereditary hemorrhagic telangiectasia resulted from a nonsense mutation Arg 479 Stop in the ALK-1 gene

ALK-1基因无义突变Arg479Stop导致的遗传性出血性毛细血管扩张症

A novel nonsense mutation in a β-thalassemia gene: β￣( 37) tgg → tag

一种新的β－地中海贫血基因&密码子37无义突变