Role of whole exome sequencing in identifying rare genetic variants in a cohort of patients presenting with congenital myopathyA. Aykanat,C. Genetti,W. Win,Z. Valivullah, E. O'Heir,B. Darras,R. Laine,A. O'Donnell-Luria,A. BeggsNEUROMUSCULAR DISORDERS(2020)引用 1|浏览5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