期刊
JOURNAL OF PEDIATRICS
卷 191, 期 -, 页码 270-274出版社
MOSBY-ELSEVIER
DOI: 10.1016/j.jpeds.2017.08.057
关键词
-
类别
资金
- Research on Measures for Intractable Diseases
- Strategic Research Program for Brain Science (SRPBS) from the Japan Agency for Medical Research and Development (AMED)
- Ministry of Education, Culture, Sports, Science and Technology of Japan (MEXT)
- Japan Society for the Promotion of Science (JSPS)
- Japan Science and Technology Agency (JST)
- Ministry of Health, Labour and Welfare
- Takeda Science Foundation
- Comprehensive Research on Disability Health and Welfare
- Grants-in-Aid for Scientific Research [16H05160] Funding Source: KAKEN
KCNT1 mutations are gain-of-function mutations in potassium channels resulting in severe infantile epilepsy. Herein we describe 3 infants with malignant migrating partial seizures with KCNT1 mutations accompanied by massive systemic to pulmonary collateral arteries with life-threatening hemoptysis and heart failure.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据