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{"target":"https://pubannotation.org/docs/sourcedb/PubMed/sourceid/8466512","sourcedb":"PubMed","sourceid":"8466512","source_url":"http://www.ncbi.nlm.nih.gov/pubmed/8466512","text":"A novel disease with deficiency of mitochondrial very-long-chain acyl-CoA dehydrogenase.\nPalmitoyl-CoA dehydrogenase activity in skin fibroblasts from seven patients with unidentified defects of fatty acid oxidation was measured in the presence and absence of antibodies against medium-chain, long-chain, and very-long-chain acyl-CoA dehydrogenases (VLCAD). Two of the patients, 4-5 month old boys, were found to have a novel disease, VLCAD deficiency, as judged from the results of very low palmitoyl-CoA dehydrogenase activity and the lack of immunoreactivity toward antibody raised to purified 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