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Biochimie|February 10, 2021
Frequent sequence variants of human glycine N-acyltransferase (GLYAT) and inborn errors of metabolismDaniel Schulke, Jörn Oliver Sass
Journal of Inherited Metabolic Disease|December 2, 2025
Human d-Glycerate Kinase, Encoded by GLYCTK and Deficient in d-Glyceric Aciduria, Is a Mitochondrial EnzymeAnne Korwitz-Reichelt, Daniel Schulke, Melanie Walter, et al.
JIMD Reports|August 1, 2025
Glycine N-Acyltransferase Deficiency due to a Homozygous Nonsense Variant in the GLYAT: A Novel Inborn Error of MetabolismMona Nourbakhsh, Mohammad Miryounesi, Ali Tale, et al.
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