NL-OMON42121招募中不适用
Clinical inventaristation and identification of (modifier) disease genes for movement disorders using next generation sequencing - Next Generation Sequencing in movement disorder
适应症
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 入组人数
- 1,000
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational
入排标准
- 年龄范围
- 12 至 99（—）
入选标准
- •Patient: Patient with diagnosis movement disorder
- •Family member: Family member of a patient with a diagnosis of movement disorder
排除标准
- •Patient: Not a patient with diagnosis movement disorder
- •Family member: Not a family member of a patient with a diagnosis movement disorder
- •No informed consent obtained for this study
- •(Severe) physical illness
- •Not being able to understand Dutch language
研究者
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