Human Genome Epidemiology Literature Finder
Rare Diseases
Records 1 - 1 (of 1 Records) |
Query Trace: Carnitine-acylcarnitine Translocase Deficiency[original query] |
---|
One potential hotspot SLC25A20 gene variants in Chinese patients with carnitine-acylcarnitine translocase deficiency. Frontiers in pediatrics 2022 11 10 1029004. Li Xiaoli, Shen Ji |
- Page last reviewed:Feb 1, 2024
- Content source: