The synthesis and characterisation of 2-methylacetoacetyl coenzyme A and its use in the identification of the site of the defect in 2-methylacetoacetic and 2-methyl-3-hydroxybutyric aciduria-Reference-Cited by-同舟云学术

The synthesis and characterisation of 2-methylacetoacetyl coenzyme A and its use in the identification of the site of the defect in 2-methylacetoacetic and 2-methyl-3-hydroxybutyric aciduria

Published:1983-03 Issue:2-3 Volume:128 Page:291-305
ISSN:0009-8981
Container-title:Clinica Chimica Acta
language:en
Short-container-title:Clinica Chimica Acta

Author:

Middleton Bruce,Bartlett Kim

Publisher

Elsevier BV

Subject

Biochemistry (medical),Clinical Biochemistry,Biochemistry,General Medicine

Reference30 articles.

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2. An inherited disorder ofisoleucine catabolisrn causing accumulation of α-methylacetoacetate and α-methyl-β-hydroxybutyrate, and intermittent metabolic acidosis;Daum;Pediatr Res,1973

3. Hyperglycinaemia with ketosis due to a defectin isoleucine metabolism: a preliminary report;Keating;Pediatrics,1972

4. Beta-ketothiolase deficiency as a cause of the ketotic hyperglycinemia syndrome;Hillman;Pediatrics,1974

5. A defect in l-isoleucine metabolism associated with α-methyl-β-hydroxybutyric and α-methylacetoacetic aciduria: quantitative in vivo and in vitro studies;Gompertz;Clin Chim Acta,1974

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