Molecular mechanisms of an inborn error of methionine pathway. Methionine adenosyltransferase deficiency.
Methionine adenosyltransferase (MAT) is a key enzyme in transmethylation, transsulfuration, and the biosynthesis of polyamines. Genetic deficiency of alpha/beta-MAT causes isolated persistent hypermethioninemia and, in some cases, unusual breath odor or neural demyelination. However, the molecular m...
Uloženo v:
| Vydáno v: | J Clin Invest |
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| Hlavní autoři: | , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
American Society for Clinical Investigation
1995
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC185831/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/7560086/ https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI118240 |
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