6号乘客
无虹膜
桑格测序
突变
先证者
遗传学
基因
生物
基因突变
分子生物学
转录因子
作者
Chuan Zhang,Shengju Hao,Qinghua Zhang,Bingbo Zhou,Furong Liu,Xiaojuan Lin,Yousheng Yan
出处
期刊:PubMed
[National Institutes of Health]
日期:2019-06-10
卷期号:36 (6): 616-619
标识
DOI:10.3760/cma.j.issn.1003-9406.2019.06.022
摘要
To identify mutation of the PAX6 gene in a patient with congenital aniridia.DNA was extracted from peripheral blood sample of the patient and analyzed by direct PCR-Sanger sequencing.The proband was found to harbor a heterozygous c.239T>A (p.Ile80Asn) mutation of the PAX6 gene. The same mutation was not found in his parents and 150 healthy controls.A novel mutation of the PAX6 gene has been identified in a sporadic case with congenital aniridia.
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