SLC12A1变异c.1684+1 G>A通过促进13号外子跳转导致巴特综合征1型
Wenke Yang1,2, Yanjun Li1, Zhenglong Guo1,2
1Henan Provincial People's Hospital, People's Hospital of Henan University, People's Hospital of Zhengzhou University, Zhengzhou, China.
Nephrology (Carlton, Vic.)
|September 11, 2024
概括
巴特特综合征1型是由SLC12A1基因突变引起的. 发现了一种新的拼接位变异,破坏了SLC12A1的功能,并扩大了这种遗传疾病的已知突变谱.
科学领域:
- 遗传学 是一个遗传学.
- 分子生物学分子生物学
- 儿科 儿科 儿科
背景情况:
- 巴特特综合征1型是一种自体相衰退性疾病.
- 它是由SLC12A1基因中的功能丧失变异引起的.
- 具有代谢性和多尿性特征,导致多水症.
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