Drögemöller Lab
Drögemöller Lab
Home
About
Team
News
Publications
Contact
Ron Wevers
Latest
Bi-allelic GOT2 mutations cause a treatable malate-aspartate shuttle-related encephalopathy
PLPHP deficiency: clinical, genetic, biochemical, and mechanistic insights
Sialic acid catabolism by N-acetylneuraminate pyruvate lyase is essential for muscle function
Exome sequencing and the management of neurometabolic disorders
Cytosolic phosphoenolpyruvate carboxykinase deficiency presenting with acute liver failure following gastroenteritis
Cite
×