在L2HGDH基因中丧失功能变异,导致L-2-氧氨酸酸尿症
Anikha Bellad1,2, Vikram V Holla3, Riyanka Kumari1,2
1Institute of Bioinformatics, International Technology Park, Bangalore, 560066, India.
Acta neurologica Belgica
|June 28, 2023
概括
基因检测发现了两个家族的L2HGDH基因中的新型L-2-Hydroxyglutaric aciduria (L2HGA) 变异. 这项研究促进了对L2HGA的理解.
科学领域:
- 生物化学 生物化学
- 遗传学 是一个遗传学.
- 神经学 神经学
背景情况:
- L-2-Hydroxyglutaric aciduria (L2HGA) 是一种罕见的,渐进的神经代谢障碍.
- 临床表现包括动力衰退,精神运动迟缓,发作,大脑衰竭和语言困难.
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