Genotype-phenotype correlations in patients with complex I deficiency due to mutations in NDUFS1 and NDUFV1Kristoffer Bjorkman,Kalliopi Sofou,Niklas Darin,Elisabeth Holme,Gittan Kollberg, Jorge Asincayuela,Karin M Holmberg Dahle,Anders Oldfors,Mar Tulinius,Alireza Moslemimag(2014)引用 23|浏览22暂无评分关键词pediatrics,clinical medicine,neurologyAI 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