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Slc22a5 haploinsufficiency does not aggravate the phenotype of the long-chain acyl-CoA dehydrogenase KO mouse
Secondary carnitine deficiency is commonly observed in inherited metabolic diseases characterized by the accumulation of acylcarnitines such as mitochondrial fatty acid oxidation (FAO) disorders. It is currently unclear if carnitine deficiency and/or acylcarnitine accumulation play a role in the pat...
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| Publicado no: | J Inherit Metab Dis |
|---|---|
| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7205564/ https://ncbi.nlm.nih.gov/pubmed/31845336 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/jimd.12204 |
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