Cloning of Dimethylglycine Dehydrogenase and a New Human Inborn Error of Metabolism, Dimethylglycine Dehydrogenase Deficiency

Dimethylglycine dehydrogenase (DMGDH) (E.C. number 1.5.99.2) is a mitochondrial matrix enzyme involved in the metabolism of choline, converting dimethylglycine to sarcosine. Sarcosine is then transformed to glycine by sarcosine dehydrogenase (E.C. number 1.5.99.1). Both enzymes use flavin adenine di...

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Detalhes bibliográficos
Main Authors: Binzak, Barbara A., Wevers, Ron A., Moolenaar, Sytske H., Lee, Yu-May, Hwu, Wuh-Liang, Poggi-Bach, Jo, Engelke, Udo F. H., Hoard, Heidi M., Vockley, Joseph G., Vockley, Jerry
Formato: Artigo
Idioma:Inglês
Publicado em: The American Society of Human Genetics 2001
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Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1275637/
https://ncbi.nlm.nih.gov/pubmed/11231903
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