一个新型的可能致病的CLCN5变体在丹特病中
S Hayward1,2, J Norton3, L Bownass4
1Bristol Medical School, Translational Health Sciences, University of Bristol, Bristol, UK.
BMC nephrology
|August 28, 2023
概括
基因分析显示,在四个患有丹特病的个体中,CLCN5基因变异存在. 这一发现重新分类了该变种,使得更快的诊断和受影响家庭的基因查成为可能.
科学领域:
- 遗传学 遗传学 是一个
- 腎臟病學 (nephrology) 是一種醫學專業.
背景情况:
- 丹特病主要是由CLCN5基因的致病变体引起的,该基因编码的是化物通道ClC-5.
- CLCN5变异导致近端管管功能障碍,这是丹特病的标志.
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