ID Database Citation 9783642403361 ISBN "Physician’s Guide to the Diagnosis, Treatment, and Follow-Up of Inherited Metabolic Diseases [Internet]. Blau N, Duran M, Gibson KM, Dionisi-Vici C. Springer; 2014. 0 p. Available from: https://books.google.com/books/about/Physician_s_Guide_to_the_Diagnosis_Treat.html?hl=&id=wJRBnwEACAAJ OpenLibrary Worldcat" 3126356 Pubmed "Urinary organic acids in succinic semialdehyde dehydrogenase deficiency: evidence of alpha-oxidation of 4-hydroxybutyric acid, interaction of succinic semialdehyde with pyruvate dehydrogenase and possible secondary inhibition of mitochondrial beta-oxidation. Brown GK, Cromby CH, Manning NJ, Pollitt RJ. J Inherit Metab Dis. 1987;10(4):367–75. PubMed Europe PMC Scholia" 16435184 Pubmed "Kinetic characterization of human hydroxyacid-oxoacid transhydrogenase: relevance to D-2-hydroxyglutaric and gamma-hydroxybutyric acidurias. Struys EA, Verhoeven NM, Ten Brink HJ, Wickenhagen WV, Gibson KM, Jakobs C. J Inherit Metab Dis. 2005;28(6):921–30. PubMed Europe PMC Scholia" 16483879 Pubmed "Metabolism of gamma-hydroxybutyrate to d-2-hydroxyglutarate in mammals: further evidence for d-2-hydroxyglutarate transhydrogenase. Struys EA, Verhoeven NM, Jansen EEW, Ten Brink HJ, Gupta M, Burlingame TG, et al. Metabolism. 2006 Mar;55(3):353–8. PubMed Europe PMC Scholia" 34244591 Pubmed "Redefining differential roles of MAO-A in dopamine degradation and MAO-B in tonic GABA synthesis. Cho HU, Kim S, Sim J, Yang S, An H, Nam MH, et al. Exp Mol Med. 2021 Jul;53(7):1148–58. PubMed Europe PMC Scholia"