Author:
Minetti C,Garavaglia B,Bado M,Invernizzi F,Bruno C,Rimoldi M,Pons R,Taroni F,Cordone G
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
Cited by
25 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献