Two Novel RRM2B Gene Mutations in a Patient with Autosomal Recessive Progressive External Ophthalmoplegia, Encephalopathy and Cytochrome C Oxidase DeficiencyNatalie S. Hauser,Renkui BaiMitochondrion（2012）引用 0|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
