无义突变能导致肌无力和囊肿纤维化等疾病。
Duchene's muscular dystrophy and cystic fibrosis are examples of hereditary diseases that result from nonsense mutations.
由此可见，反义pna有可能在靶基因区域显著性抑制无义突变。
Thus, it is possible to significantly suppress nonsense mutations within target genes using antisense PNAs.
结论PINK1基因R 492x无义突变不大可能是中国散发性帕金森病患者的突变热点。
Conclusion R492X nonsense mutation of PINK1 gene was rare in Chinese sporadic patients with PD.
由于人体细胞的无义突变也可能敏感于反义试剂的抑制作用，这就为治疗由于无义突变导致的多种疾病提供了一个新途径。
Nonsense termination in human cells may also be susceptible to suppression by antisense agents, providing a new approach to address numerous diseases caused by nonsense mutations.
由于人体细胞的无义突变也可能敏感于反义试剂的抑制作用，这就为治疗由于无义突变导致的多种疾病提供了一个新途径。
Nonsense termination in human cells may also be susceptible to suppression by antisense agents, providing a new approach to address numerous diseases caused by nonsense mutations.
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