
D-Glyceric aciduria: is GLYCTK really mitochondrial?
From JIMD Podcasts by Journal of Inherited Metabolic Disease
March 31, 2026 · 17 min
About this episode
Jörn Oliver Sass discusses the implications of D-glyceric aciduria and the role of GLYCTK in mitochondrial function.
A rare disorder, a surprisingly basic biological question, and a paper that revisits what GLYCTK actually does. Jörn Oliver Sass joins the podcast to discuss D-glyceric aciduria, mitochondrial localization of D-glycerate kinase, and why getting the fundamentals right still matters. Human D-Glycerate Kinase, Encoded by GLYCTK and Deficient in D-Glyceric Aciduria, Is a Mitochondrial Enzyme Anne Korwitz-Reichelt, et al https://doi.org/10.1002/jimd.70119
People in this episode
Guest: Jörn Oliver Sass
Topics covered
- D-glyceric aciduria
- mitochondrial localization
- D-glycerate kinase
- biological questions
- fundamentals in biology
Keywords
- D-glyceric aciduria
- GLYCTK
- mitochondrial enzyme
- D-glycerate kinase
- biological fundamentals
Mentioned in this episode
Organizations: Journal of Inherited Metabolic Disease, GLYCTK
Books & works: Human D-Glycerate Kinase, Encoded by GLYCTK and Deficient in D-Glyceric Aciduria, Is a Mitochondrial Enzyme
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