Ann Child Neurol.
2021 Oct;29(4):194-198. 10.26815/acn.2021.00416.
A Case of Mitochondrial Trifunctional Protein Deficiency with HADHB Variants Diagnosed Using Whole-Exome Sequencing
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- 1Department of Pediatrics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea
- KMID: 2526112
- DOI: http://doi.org/10.26815/acn.2021.00416
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