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About this Biochemistry, Genetics and Molecular Biology article
Mutations in mitochondrially encoded complex I enzyme as the second common cause in a cohort of Chinese patients with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes by Zhao, Danhua; Hong, Daojun; Zhang, Wei; Yao, Sheng; Qi, Xiaokun; Lv, He; Zheng, Riliang; Feng, Liqun; Huang, Yining; Yuan, Yun; Wang, Zhaoxia is a Biochemistry, Genetics and Molecular Biology article available to read on EtoBox.
It is typically read by researchers, students, and practitioners in Biochemistry, Genetics and Molecular Biology.
- Author
- Zhao, Danhua; Hong, Daojun; Zhang, Wei; Yao, Sheng; Qi, Xiaokun; Lv, He; Zheng, Riliang; Feng, Liqun; Huang, Yining; Yuan, Yun; Wang, Zhaoxia
- Publisher
- Nature Publishing Group; Springer Science and Business Media LLC; Springer Verlag (ISSN 1435-232X)
- Published
- 2011
- Language
- EN
- Field
- Biochemistry, Genetics and Molecular Biology (Life Sciences)