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...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Prif Awduron: Wang, Wei, Mohsen, Al-Walid, Uechi, Guy, Schreiber, Emanuel, Balasubramani, Manimalha, Day, Billy, Barmada, M. Michael, Vockley, Jerry
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: 2014
Pynciau:
Article
Mynediad Ar-lein: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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