A de novo mutation in SMC1A gene identified in a Chinese infant with nonclassical Cornelia de Lange syndrome and drug-resistant epilepsyHongjun Fang,Xi Zhang,Bo Xiao,Lily Zhang,Hongyu LongNeurological Sciences（2020）引用 1|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
