AAV-CRISPR/Cas9 Gene Editing is Therapeutic in a Novel, Humanized Mouse Model of GUCY2D-Associated Cone Rod Dystrophy (CORD6)Russell W. Mellen,K. Tyler McCullough,Diego Fajardo,Kaitlyn Calabro,Sean Crosson,Emily Xu,Sanford L. Boye,Shannon E. BoyeMOLECULAR THERAPY(2022)引用 0|浏览4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