scholarly article | Q13442814 |
P6179 | Dimensions Publication ID | 1039561618 |
P356 | DOI | 10.1007/BF02263600 |
P698 | PubMed publication ID | 6790857 |
P2093 | author name string | R Smith | |
A Green | |||
R J Pollitt | |||
P J Congdon | |||
D Haigh | |||
P2860 | cites work | 13CValine metabolism in methylmalonicacidemia using nuclear magnetic resonance: propinonate as an obligate intermediate | Q35089675 |
The determination of β-aminoisobutyric acid in human serum by ion-exchange chromatography | Q66916399 | ||
P433 | issue | 2 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 79-80 | |
P577 | publication date | 1981-01-01 | |
P1433 | published in | Journal of Inherited Metabolic Disease | Q6295359 |
P1476 | title | Hypermethioninaemia and 3-hydroxyisobutyric aciduria in an apparently healthy baby | |
P478 | volume | 4 |
Q34210330 | 3-Hydroxyisobutyrate aciduria and mutations in the ALDH6A1 gene coding for methylmalonate semialdehyde dehydrogenase |
Q27675880 | Biochemical and Structural Studies of Uncharacterized Protein PA0743 from Pseudomonas aeruginosa Revealed NAD+-dependent L-Serine Dehydrogenase |
Q34195960 | Excessive excretion of beta-alanine and of 3-hydroxypropionic, R- and S-3-aminoisobutyric, R- and S-3-hydroxyisobutyric and S-2-(hydroxymethyl)butyric acids probably due to a defect in the metabolism of the corresponding malonic semialdehydes |
Q30445321 | Isolated persistent hypermethioninemia. |
Q33837763 | Molecular genetics of hepatic methionine adenosyltransferase deficiency |