Excessive excretion of β-alanine and of 3-hydroxypropionic,R- andS-3-aminoisobutyric,R- andS-3-hydroxyisobutyric andS-2-(hydroxymethyl)butyric acids probably due to a defect in the metabolism of the corresponding malonic semialdehydes-Reference-Cited by-同舟云学术

Excessive excretion of β-alanine and of 3-hydroxypropionic,R- andS-3-aminoisobutyric,R- andS-3-hydroxyisobutyric andS-2-(hydroxymethyl)butyric acids probably due to a defect in the metabolism of the corresponding malonic semialdehydes

Published:1985-06 Issue:2 Volume:8 Page:75-79
ISSN:0141-8955
Container-title:Journal of Inherited Metabolic Disease
language:en
Short-container-title:J Inherit Metab Dis

Author:

Pollitt R. J.,Green A.,Smith R.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://www.springerlink.com/index/pdf/10.1007/BF01801669

Reference20 articles.

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2. Baretz, B. H. and Tanaka, K. Metabolism in ratsin vivo of isobutyrates labeled with stable isotopes at various positions. Identification of propionate as an obligate intermediate.J. Biol. Chem. 253 (1978) 4203–4213

3. Baretz, B. H., Lollo, C. P. and Tanaka, K. Metabolism in ratsin vivo ofRS-2-methylbutyrate andn-butyrate labeled with stable isotopes at various positions.J. Biol. Chem. 254 (1979) 3468–3478

4. Congden, P. J., Haigh, D., Smith, R., Green, A. and Pollitt, R. J. Hypermethioninaemia and 3-hydroxyisobutyric aciduria in an apparently healthy baby.J. Inher. Metab. Dis. 4 (1981) 79–80

5. Gaull, G. E., Bender, A. N., Vulovic, D., Tallan, H. H. and Schaffner, F. Methioninemia and myopathy: A new disorder.Ann. Neurol. 9 (1981) 423–432

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