NL-OMON41692已完成不适用
A novel causative gene of congenital central hypothyroidism. - Gene mutations in central hypothyroidism.
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 50
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
- 2 至 99（—）
入选标准
- •- Congenital central hypothyroidism.
- •- First- or second-degree relative of a patient with congenital central hypothyroidism.
排除标准
- •Carriers of other genetic defects known to cause congenital central hypothyroidism.
研究者
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