Very-long-chain acyl-coenzyme A dehydrogenase deficiency in a child with recurrent myoglobinuria

Author:

Minetti C,Garavaglia B,Bado M,Invernizzi F,Bruno C,Rimoldi M,Pons R,Taroni F,Cordone G

Publisher

Elsevier BV

Subject

Genetics(clinical),Clinical Neurology,Neurology,Pediatrics, Perinatology, and Child Health

Reference14 articles.

1. Very long acyl-CoA dehydrogenase deficiency: identification of a new inborn error of mitochondrial fatty acid oxidation in fibroblasts;Bertrand;Biochem Biophys Acta,1993

2. Cloning of human very-long-chain acyl coenzyme A dehydrogenase and molecular characterization of its deficiency in two patients;Aoyama;Am J Hum Genet,1995

3. Fatty-acid mitochondrial b-oxidation and hypoglycemia in children;Taroni;Curr Opin Neurol,1996

4. Cloning and characterization of human very-long-chain acyl-CoA dehydrogenase cDNA, chromosomal assignment of the gene and identification in four patients of nine different mutations within the VLCAD gene;Andresen;Hum Mol Genet,1996

5. Very-long-chain acyl coenzyme A dehydrogenase deficiency presenting with exercise-induced myoglobinuria;Ogilvie;Neurology,1994

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4. Rhabdomyolysis in a neonate due to very long chain acyl CoA dehydrogenase deficiency;Molecular Genetics and Metabolism Reports;2015-06

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