Fingerprint
Dive into the research topics of 'FBXL4 defects are common in patients with congenital lactic acidemia and encephalomyopathic mitochondrial DNA depletion syndrome'. Together they form a unique fingerprint.- Sort by
- Weight
- Alphabetically
FBXL4 defects are common in patients with congenital lactic acidemia and encephalomyopathic mitochondrial DNA depletion syndrome
H. Dai, V. W. Zhang, A. W. El-Hattab, C. Ficicioglu, M. Shinawi, M. Lines, A. Schulze, M. Mcnutt, G. Gotway, X. Tian, S. Chen, J. Wang, W. J. Craigen, L. J. Wong
Research output: Contribution to journal › Article › peer-review
15
Scopus
citations