P573: Biallelic missense NEXN variants lead to recessive severe neonatal cardiomyopathy Casey Thornton,Elizabeth Mizerik, Dan Brooks,Chaya Murali, Christian Parobek,Lorraine Potocki,Pengfei Liu, Nichole Owen,Liesbeth VossaertGenetics in Medicine Open（2023）引用 0|浏览8暂无评分关键词biallelic missense nexn variants,severe neonatal,p573AI 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
