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Unique plasma metabolomic signatures of individuals with inherited disorders of long-chain fatty acid oxidation
Blood and urine acylcarnitine profiles are commonly used to diagnose long-chain fatty acid oxidation disorders (FAOD: i.e., long-chain hydroxy-acyl-CoA dehydrogenase [LCHAD] and carnitine palmitoyltransferase 2 [CPT2] deficiency), but the global metabolic impact of long-chain FAOD has not been repor...
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| Publicado no: | J Inherit Metab Dis |
|---|---|
| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4851894/ https://ncbi.nlm.nih.gov/pubmed/26907176 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s10545-016-9915-3 |
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