The molecular basis of pediatric long chain 3-hydroxyacyl-CoA dehydrogenase deficiency associated with maternal acute fatty liver of pregnancy

Biochemistry, Genetics and Molecular Biology

• Allele 100%
• 3-Hydroxyacyl-CoA Dehydrogenase 100%
• Acute Fatty Liver of Pregnancy 100%
• Oxidoreductase 66%
• Conformation 33%
• Enzyme 33%
• Progeny 33%
• C-Terminus 33%
• Glutamine 33%
• Alpha Oxidation 33%
• Protein Subunit 33%
• Exon 33%
• Dehydrogenase 33%
• Codon 33%
• Beta Oxidation 33%
• Glutamic Acid 33%
• Enzyme Metabolism 33%
• Mitochondrial Trifunctional Protein 33%

Keyphrases

• LCHAD 100%
• Acute Fatty Liver 100%
• Mitochondrial Trifunctional Protein 75%
• LCHAD Deficiency 50%
• Skeletal Myopathy 25%
• Sudden Unexplained Death 25%
• Acute Hepatic Encephalopathy 25%
• Abnormal Liver Enzymes 25%
• Reye Syndrome 25%
• Cardiomyopathy 25%
• Glutamic Acid 25%
• Third child 25%
• Long-chain Fatty Acid Oxidation 25%
• Families with children 25%
• Sudden Unexplained Death in childhood 25%