Pyruvate dehydrogenase subcomplex with lipoamide dehydrogenase deficiency in a patient with lactic acidosis and branched chain ketoaciduria-Reference-Cited by-同舟云学术

Pyruvate dehydrogenase subcomplex with lipoamide dehydrogenase deficiency in a patient with lactic acidosis and branched chain ketoaciduria

Published:1984-06 Issue:1 Volume:140 Page:59-64
ISSN:0009-8981
Container-title:Clinica Chimica Acta
language:en
Short-container-title:Clinica Chimica Acta

Author:

Sadayuki Matuda,Akito Kitano,Yusuke Sakaguchi,Makoto Yoshino,Takeyori Saheki

Publisher

Elsevier BV

Subject

Biochemistry, medical,Clinical Biochemistry,Biochemistry,General Medicine

Reference24 articles.

1. Lipoamide dehydrogenase;Charles,1976

2. Purification and characterization of branched chain α-ketoacid dehydrogenase from bovine liver mitochondria;Danner;J Biol Chem,1979

3. Mammalian α-ketoacid dehydrogenase complex. VII. Resolution and reconstitution of the pig heart 2-oxoglutarate dehydrogenase complex;Tanaka;J Biol Chem,1972

4. α-Keto acid dehydrogenase complexes. XV. Purification and properties of the component enzymes of the pyruvate dehydrogenase complex from bovine kidney and heart;Linn;Arch Biochem Biophys,1972

5. A defect in pyruvate decarboxylase in a child with an intermittent movement disorder;Blass;J Clin Invest,1970

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