NL-OMON48953招募中不适用
STXBP1-Encephalopathy: a multifaceted cohort study into the clinical, electroencephalographical and cellular profile of STXBP1-E patients - STXBP1-E: A multilevel investigation
Functionele Genoomanalyse, Klinische Genetica0 个研究点目标入组 25 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
- 25
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational invasive
入排标准
- 年龄范围
- 2 至 99（—）
入选标准
- •Identified mutation in the STXBP1-gene
排除标准
- •Severe language barrier that is likely to hinder the procedure of informed consent.
研究者
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