Development of a CRISPR/Cas9-mediated gene editing platform to restore the reading frame for 60% of Duchenne muscular dystrophy patientsC. Young, M. Hicks,Natalia Ermolova,H. Nakano,M. Jan, S. Younesi,Stanley F. Nelson, C. Miceli,A. Pyle,Melissa J. SpencerNEUROMUSCULAR DISORDERS（2016）引用 0|浏览16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
