| 标题 |
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 |
| 网址 | |
| DOI | |
| 其它 |
期刊:Journal of Human Genetics 作者:Dan-Hua Zhao; D. Hong; Wei Zhang; S. Yao; X. Qi; et al 出版日期:2011-11-01 |
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(2025-6-4)