An explanation for metabolite excretion in high- and low-excretor patients with glutaric acidemia type 1

Mol Genet Metab. 2019 Aug;127(4):325-326. doi: 10.1016/j.ymgme.2019.07.005. Epub 2019 Jul 11.

Authors

Stephen I Goodman¹, Michael Woontner²

Affiliations

¹ Department of Pediatrics, University of Colorado School of Medicine, USA. Electronic address: stephen.goodman@ucdenver.edu.
² Department of Pediatrics, University of Colorado School of Medicine, USA.

PMID: 31324527
DOI: 10.1016/j.ymgme.2019.07.005

No abstract available

MeSH terms

Amino Acid Metabolism, Inborn Errors / genetics
Amino Acid Metabolism, Inborn Errors / metabolism*
Brain Diseases, Metabolic / genetics
Brain Diseases, Metabolic / metabolism*
Glutarates / metabolism*
Glutaryl-CoA Dehydrogenase / deficiency*
Glutaryl-CoA Dehydrogenase / genetics*
Glutaryl-CoA Dehydrogenase / metabolism
Humans

Substances

Glutarates
Glutaryl-CoA Dehydrogenase

Supplementary concepts

Glutaric Acidemia I