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...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Päätekijät: Ubagai, T, Lei, K J, Huang, S, Mudd, S H, Levy, H L, Chou, J Y
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 1995
Aiheet:
Research Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC185831/
https://ncbi.nlm.nih.gov/pubmed/7560086
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