Primary Carnitine Deficiency Due to a Failure of Carnitine Transport in Kidney, Muscle, and Fibroblasts

Keyphrases

• Kidney 100%
• Fibroblasts 100%
• Carnitine Deficiency 100%
• Mitochondria 33%
• Fatty Acids 33%
• Coma 33%
• Early childhood 33%
• Inner Mitochondrial Membrane 33%
• Fatty Acid Oxidation 33%
• Recurrent Episodes 33%
• Hypoglycemia 33%
• L-carnitine 33%
• Long-chain Fatty Acids 33%

Biochemistry, Genetics and Molecular Biology

• Fibroblast 100%
• Alpha Oxidation 100%
• Mitochondrion 50%
• Inner Mitochondrial Membrane 50%
• Infancy 50%
• Beta Oxidation 50%
• Coma 50%