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-Reference-Cited by-同舟云学术

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

Published:2011-08-18 Issue:11 Volume:56 Page:759-764
ISSN:1434-5161
Container-title:Journal of Human Genetics
language:en
Short-container-title:J Hum Genet

Author:

Zhao Danhua,Hong Daojun,Zhang Wei,Yao Sheng,Qi Xiaokun,Lv He,Zheng Riliang,Feng Liqun,Huang Yining,Yuan Yun,Wang Zhaoxia

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://www.nature.com/articles/jhg201196.pdf

Reference42 articles.

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2. DiMauro, S. & Schon, E. A. Mitochondrial respiratory-chain diseases. N. Engl. J. Med. 348, 2656–2668 (2003).

3. Zeviani, M. & Carelli, V. Mitochondrial disorders. Curr. Opin. Neurol. 16, 585–594 (2003).

4. Anderson, S., Bankier, A. T., Barrell, B. G., de Bruijn, M. H., Coulson, A. R., Drouin, J. et al. Sequence and organization of the human mitochondrial genome. Nature 290, 457–465 (1981).

5. Goto, Y., Nonaka, I. & Horai, S. Mutation in the tRNA(Leu)(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies. Nature 348, 651–653 (1990).

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