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Fasting induces prominent proteomic changes in liver in very long chain Acyl-CoA dehydrogenase deficient mice
Very long chain acyl-CoA dehydrogenase (VLCAD) deficiency (VLCADD) is a clinically heterogeneous disorder of mitochondrial fatty acid β-oxidation usually identified through newborn screening. Genotype-phenotype correlations have been defined, but considerable clinical heterogeneity still exists. Sym...
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| Gepubliceerd in: | Biochem Biophys Rep |
|---|---|
| Hoofdauteurs: | , , , , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
Elsevier
2016
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5613767/ https://ncbi.nlm.nih.gov/pubmed/28955973 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.bbrep.2016.08.014 |
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