NL-OMON41857招募中不适用
Whole exome sequencing to unravel the genetics of neuralgic amyotrophy - Genetics of neuralgic amyotrophy
eurologie0 个研究点目标入组 250 人开始时间: 待定最近更新:
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 发起方
- 入组人数
- 250
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
- 18 至 64（—）
入选标准
- •- NA patients known in the RUN Medical Centre
- •- (Un)affected relatives of patients with NA in whom a de novo mutation has been identified
- •- Informed consent
排除标准
- •- Patients under the age of 18 years
- •- Incompetent patients
研究者
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