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...

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Veröffentlicht in:	J Clin Invest
Hauptverfasser:	Ubagai, T, Lei, K J, Huang, S, Mudd, S H, Levy, H L, Chou, J Y
Format:	Artigo
Sprache:	Inglês
Veröffentlicht:	American Society for Clinical Investigation 1995
Schlagworte:	Research Article
Online-Zugang:	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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