Biochemical characterization of human D-2-hydroxyglutarate dehydrogenase and two disease related variants reveals the molecular cause of D-2 hydroxyglutaric aciduria

Marina Toplak; Julia Brunner; Julia Schmidt; Peter Macheroux

doi:https://doi.org/10.1016/j.bbapap.2019.07.008

Biochemical characterization of human D-2-hydroxyglutarate dehydrogenase and two disease related variants reveals the molecular cause of D-2 hydroxyglutaric aciduria

Marina Toplak, Julia Brunner, Julia Schmidt, Peter Macheroux

Institute of Biochemistry (6480)

Research output: Contribution to journal › Article › peer-review

Original language	English
Journal	Biochimica et Biophysica Acta / Proteins and Proteomics
Volume	1867
Issue number	140255
DOIs	https://doi.org/10.1016/j.bbapap.2019.07.008
Publication status	Published - 23 Jul 2019

Keywords

electron transferring flavoprotein
D-2-hydroxyglutaric aciduria
D-2-hydroxyglutarate
D-lactate

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

Access to Document

https://doi.org/10.1016/j.bbapap.2019.07.008Licence: CC BY-NC-ND 4.0

Cite this

Biochemical characterization of human D-2-hydroxyglutarate dehydrogenase and two disease related variants reveals the molecular cause of D-2 hydroxyglutaric aciduria. / Toplak, Marina; Brunner, Julia; Schmidt, Julia et al.
In: Biochimica et Biophysica Acta / Proteins and Proteomics, Vol. 1867, No. 140255, 23.07.2019.

Research output: Contribution to journal › Article › peer-review

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