Clinical and genetic spectrum of pediatric mitochondrial disorders in China: insights from a 47-case genetically confirmed cohort
中国儿童线粒体疾病的临床和遗传谱:来自47例基因确诊病例队列的启示
期刊:Orphanet Journal of Rare Diseases
影响因子:3.5
doi:10.1186/s13023-025-04180-7
Yang, Fan; Yao, Ruen; Chang, Guoying; Hu, Jiayue; Feng, Biyun; Wang, Libo; Hu, Feihan; Huang, Yiguo; Wu, Shuo; Yu, Tingting; Ding, Yu; Wang, Xiumin