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1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
