Biallelic variants in ASCC3 expand the phenotypic spectrum of congenital myasthenic syndromesM. Johari, I Herman,K. Polavarapu,A. Nalini,J. Lupski, A. Topf,M. Villanova,G. Tasca,E. Mercuri, E. Pegoraro, M. Sivasankar, V Straub,E. Malfatti, H. Lochmuller,D. Calame,G. RavenscroftNEUROMUSCULAR DISORDERS(2022)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