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Complex changes in the liver mitochondrial proteome of short chain acyl-CoA dehydrogenase deficient mice
Short-chain acyl-CoA dehydrogenase (SCAD) deficiency is an autosomal recessive inborn error of metabolism that leads to the impaired mitochondrial fatty acid β-oxidation of short chain fatty acids. It is heterogeneous in clinical presentation including asymptomatic in most patients identified by new...
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| Glavni autori: | , , , , , , , |
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| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
2014
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| Teme: | |
| Online pristup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4167795/ https://ncbi.nlm.nih.gov/pubmed/24685553 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ymgme.2014.02.014 |
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