Author:
Schmiesing Jessica,Lohmöller Benjamin,Schweizer Michaela,Tidow Henning,Gersting Søren W.,Muntau Ania C.,Braulke Thomas,Mühlhausen Chris
Publisher
Oxford University Press (OUP)
Subject
Genetics (clinical),Genetics,Molecular Biology,General Medicine
Reference52 articles.
1. Goodman S.I. Frerman F.E. (2001) Organic acidemias due to defects in lysine oxidation: 2-ketoadipic acidemia and glutaric acidemia. In Scriver C.R. Beaudet A.L. Sly W.S. Valle D. Childs B. Kinzler K.W. Vogelstein B. (eds.), The Metabolic and Molecular Bases of Inherited Disease. McGraw-Hill Inc., New York, USA, pp. 2195–2204.
2. Crystal Structures of Human Glutaryl-CoA Dehydrogenase with and without an Alternate Substrate: Structural Bases of Dehydrogenation and Decarboxylation Reactions,
3. Structure and mechanism of action of the acyl-CoA dehydrogenases;Thorpe;Faseb J,1995
4. The unsolved puzzle of neuropathogenesis in glutaric aciduria type I;Jafari;Mol. Genet. Metab,2011
5. Maintenance treatment of glutaryl-CoA dehydrogenase deficiency
Cited by
16 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