3-Hydroxyacyl-CoA dehydrogenase (HAD) deficiency replaces short-chain hydroxyacyl-CoA dehydrogenase (SCHAD) deficiency as well as medium- and short-chain hydroxyacyl-CoA dehydrogenase (M/SCHAD) deficiency as the consensus name of this fatty acid oxidation disorder-Reference-Cited by-同舟云学术

3-Hydroxyacyl-CoA dehydrogenase (HAD) deficiency replaces short-chain hydroxyacyl-CoA dehydrogenase (SCHAD) deficiency as well as medium- and short-chain hydroxyacyl-CoA dehydrogenase (M/SCHAD) deficiency as the consensus name of this fatty acid oxidation disorder

Published:2007-06 Issue:2 Volume:91 Page:205-206
ISSN:1096-7192
Container-title:Molecular Genetics and Metabolism
language:en
Short-container-title:Molecular Genetics and Metabolism

Author:

He Xue-Ying,Yang Song-Yu

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference10 articles.

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2. Molecular mechanisms of the fatty acid β-oxidation enzyme catalysis;Yang;Adv. Exp. Med. Biol.,1999

3. Impact of the intramitochondrial enzyme organization on fatty acid oxidation;Liang;Biochem. Soc. Trans.,2001

4. Human short-chain l-3-hydroxyacyl-CoA dehydogenase: cloning and characterization of the coding sequence;Vredendaal;Biochem. Biophys. Res. Commun.,1996

5. Short-chain l-3-hydroxyacyl-CoA dehydrogenase deficiency in muscle: a new cause of recurrent myoglobinuria and encephalopathy;Tien;Ann. Neurol.,1991

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