| 标题 |
FBXL4 defects are common in patients with congenital lactic acidemia and encephalomyopathic mitochondrial DNA depletion syndrome |
| 网址 | |
| DOI | |
| 其它 |
期刊:Clinical Genetics 作者:Hongzheng Dai; V. Zhang; Ayman W El-Hattab; Can Ficicioglu; M. Shinawi; et al 出版日期:2017-04-01 |
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(2025-6-4)