Author:
Bijarnia S.,Wiley V.,Carpenter K.,Christodoulou J.,Ellaway C. J.,Wilcken B.
Subject
Genetics(clinical),Genetics
Reference11 articles.
1. Christensen E (1983) Improved assay of glutaryl CoA dehydrogenase in cultured cells and liver. Clin Chim Acta 129: 91–97.
2. Goodman SI, Freeman FE (2001) Organic acidemias due to defects in lysine oxidation: 2-ketoadipic acidemia and glutaric acidemia. In: Scriver CR, Beaudet AL, Sly WS, Valle D, eds; Childs B, Kinzler KW, Vogelstein B, assoc. eds. The Metabolic and Molecular Bases of Inherited Disease, 8th edn. New York: McGraw-Hill, 2195–2204.
3. Goodman SI, Markey SP, Moe PG, Miles BS, Teng CC (1975) Glutaric aciduria: a ‘new’ disorder of amino acid metabolism. Biochem Med 12: 12–21.
4. Kölker S, Garbade SF, Greenberg CR, et al (2006) Natural history, outcome and therapeutic efficacy in children and adults with glutaryl-CoA dehydrogenase deficiency. Pediatr Res 59: 840–847.
5. Kölker S, Christensen E, Leonard JV, et al (2007a) Guideline for the diagnosis and management. J Inherit Metab Dis 30: 5–22.
Cited by
53 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献