Mosaicism of de novo SCN1A mutations in epilepsy: an explanation for variable phenotypes? I. M. De lange,M. Koudijs,R. van't Slot,F. Mulder, E. C. Carbo,M. van Kempen,B. Gunning, L. van Gemert,A. Sonsma,S. Savelberg, N. Knoers,E. Brilstra,B. KoelemanEUROPEAN JOURNAL OF HUMAN GENETICS(2018)引用 0|浏览7暂无评分AI 理解论文溯源树样例生成溯源树,研究论文发展脉络Chat Paper正在生成论文摘要