Identification of a novel deletion mutation in PHKA2 in a taiwanese patient with type IXa glycogen storage disease.Wei-De Lin,Fuu-Jen Tsai,Chung-Hsing WangPediatrics and neonatology（2023）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
