Pregnancy complications are frequent in long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency
Author:
Publisher
Elsevier BV
Subject
Obstetrics and Gynaecology
Reference21 articles.
1. Acute fatty liver of pregnancy and long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency;Treem;Hepatology,1994
2. Pregnancy and fetal long-chain 3-hydroxyacyl coenzyme A dehydrogenase deficiency;Wilcken;Lancet,1993
3. Novel fatty acid β-oxidation enzymes in rat liver mitochondria, II: purification and properties of enoyl-coenzyme A (CoA) hydratase/3-hydroxyacyl-CoA dehydrogenase/3-ketoacyl-CoA thiolase trifunctional protein;Uchida;J Biol Chem,1992
4. Human liver long-chain 3-hydroxyacyl-coenzyme A dehydrogenase is a multifunctional membrane-bound beta-oxidation enzyme of mitochondria;Carpenter;Biochem Biophys Res Commun,1992
5. Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: high frequency of the G1528C mutation with no apparent correlation with the clinical phenotype;IJlst;J Inher Metab Dis,1995
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