桑格测序
错义突变
遗传学
遗传变异
生物
基因
生物信息学
疾病
拷贝数变化
疾病基因鉴定
突变
医学
基因组
外显子组测序
内科学
作者
Fei Xie,Xiaosheng Zheng,Zhidong Cen,Wei Luo
出处
期刊:PubMed
日期:2019-10-10
卷期号:36 (10): 957-960
标识
DOI:10.3760/cma.j.issn.1003-9406.2019.10.002
摘要
To explore the genetic basis of a patient with early-onset Parkinson disease from a consanguineous family.Homozygosity mapping and Sanger sequencing of cDNA were used to identify the causative mutation.A homozygous missense variation (c.56C>G, p.Thr19Arg) in the PARK7 gene was identified in the patient. In silico analysis suggested the c.56C>G variation to be pathogenic.Homozygous c.56C>G variation of the PARK7 gene was the disease-causing variation in this family.
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