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Comparison of clinical, magnetic resonance and evoked potentials data in a case of valproic-acid-related hyperammonemic coma
Hereditary or acquired defects in the transport mechanisms are the major cause of LC deficiency, leading to pathologies such as cardiomyopathy and skeletal muscle myopathy
[13] Metabolic defects of fatty acid oxidation [edit] More than 20 human genetic defects in fatty acid transport or oxidation have been identified
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