Molecular basis of human mitochondrial very-long-chain acyl-CoA dehydrogenase deficiency causing cardiomyopathy and sudden death in childhood

Medicine and Dentistry

• Acyl-CoA 25%
• Arginine 25%
• Base 50%
• Cardiomyopathy 100%
• Childhood 75%
• Complementary DNA 25%
• Consensus 25%
• Death 25%
• Dinucleotide 25%
• Donor 25%
• Enzyme 25%
• Exon 100%
• Fatty Acid Oxidation 25%
• Gene 25%
• Heart 25%
• Heart Arrest 25%
• Hepatic Encephalopathy 25%
• Heterozygote 50%
• Intron 25%
• Liver Failure 25%
• Long Chain Acyl Coenzyme A Dehydrogenase 50%
• Long Chain Fatty Acid 25%
• Messenger RNA 25%
• Missense Mutation 25%
• Myopathy 25%
• Nucleotide Sequence 25%
• Oxidoreductase 25%
• Patient 50%
• Polymerase Chain Reaction 25%
• Sudden Death 50%
• Tryptophan 25%

Biochemistry, Genetics and Molecular Biology

• Acyl-CoA 25%
• Allele 25%
• Alpha Oxidation 75%
• Arginine 25%
• Beta Oxidation 25%
• Cardiac Arrest 25%
• Childhood 75%
• Consensus 25%
• Energy 25%
• Energy Yield 25%
• Exon 100%
• Fatty Acid 25%
• Genetic Carrier 25%
• Intron 25%
• Lysozyme 25%
• Messenger RNA 25%
• Missense Mutation 25%
• Mutation 75%
• Nested Gene 25%
• Nucleotide Sequence 25%
• Oxidoreductase 25%
• Polymerase Chain Reaction 25%
• Tryptophan 25%
• Very-Long-Chain Acyl-CoA Dehydrogenase 50%