KMT2C pathogenic variants result in a neurodevelopmental disorder with distinct clinical and DNA methylation featuresDmitrijs Rots,Sanaa Choufani,Victor Faundes,Alexander Dingemans, Lisenka Vissers,Tjitske Kleefstra,Siddharth Banka,Rosanna WeksbergEUROPEAN JOURNAL OF HUMAN GENETICS(2024)引用 0|浏览0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