Novel ST3GAL3 mutations in three patients with intellectual disability and epilepsyL. Ruaud,D. Heron,H. Maurey, C. Mehler-Jacob,D. Doummar,S. Heide,C. Nava,B. Keren,C. MignotEUROPEAN JOURNAL OF HUMAN GENETICS(2019)引用 0|浏览37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