Browsing by Author Wei, Xiujuan
Showing results 1 to 4 of 4
Issue Date |
Title |
Author(s) |
Mar-2020 |
Mutations in TOMM70 lead to multi-OXPHOS deficiencies and cause severe anemia, lactic acidosis, and developmental delay |
Wei, Xiujuan;Du, Miaomiao;Xie, Jie;Luo, Ting;Zhou, Yan;Zhang, Kun;Li, Jin;Chen, Deyu;Xu, Pu;Jia, Manli;Zhou, Huaibin;Fang, Hezhi;Lyu, Jianxin;Yang, Yanling |
Nov-2020 |
A novel mitochondrial m.14430A > G (MT-ND6, p.W82R) variant causes complex I deficiency and mitochondrial Leigh syndrome |
Du, Miaomiao;Wei, Xiujuan;Xu, Pu;Xie, Anran;Zhou, Xiyue;Yang, Yanling;Li, Dongxiao;Lyu, Jianxin;Fang, Hezhi |
2018 |
SURF1 mutations in Chinese patients with Leigh syndrome: Novel mutations, mutation spectrum, and the functional consequences |
Li, Yuanyuan;Wen, Shumeng;Li, Dongxiao;Xie, Jie;Wei, Xiujuan;Li, Xiyuan;Liu, Yi;Fang, Hezhi;Yang, Yanling;Lyu, Jianxin |
Mar-2020 |
Systematic analysis of a mitochondrial disease-causing ND6 mutation in mitochondrial deficiency |
Chen, Deyu;Zhao, Qiongya;Xiong, Jingting;Lou, Xiaoting;Han, Qinxia;Wei, Xiujuan;Xie, Jie;Li, Xueyun;Zhou, Huaibin;Shen, Lijun;Yang, Yanling;Fang, Hezhi;Lyu, Jianxin |