PINK1造句

Screening and Confirmation of Proteins Interacting with PINK1

Conclusion R492X nonsense mutation of PINK1 gene was rare in Chinese sporadic patients with PD.

结论PINK1基因R 492x无义突变不大可能是*散发*帕金森病患者的突变热点。

方法应用聚合酶链反应（ PCR）、DNA测序和限制*片段长度多态*（RFLP）等技术对1个帕金森病家系及120例散发*帕金森病患者进行PINK1基因R492X的突变分析。