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Combined enzyme defect of mitochondrial fatty acid oxidation.
A young girl presented with recurrent episodes of muscle weakness culminating in a severe attack of generalized muscle weakness. In the muscle mitochondria from the patient there was an abnormal pattern of intermediates of beta-oxidation with an accumulation of 3-hydroxyacyl- and 2-enoyl-CoA and car...
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| Main Authors: | , , , , , , , |
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| Formato: | Artigo |
| Idioma: | en |
| Publicado em: |
1992
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC443162/ https://ncbi.nlm.nih.gov/pubmed/1401059 |
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