[与SLC6A8基因变异相关的肌酸载体缺乏症的临床特征]
1Department of Neurology, Neurological Center, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing100045, China.
Zhonghua er ke za zhi = Chinese journal of pediatrics
|November 20, 2024
概括
由SLC6A8基因变异引起的肌酸载体 (CRTR) 缺乏导致发育延迟和发作. 诊断包括评估临床特征,脑部成像和对这种罕见疾病的基因检测.
科学领域:
- 神经学 神经学
- 遗传学 是一个遗传学.
- 代谢障碍 代谢障碍 代谢障碍
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