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Adult-onset Very Long-Chain Acyl-CoA Dehydrogenase Deficiency (VLCADD)
BACKGROUND: Very long-chain acyl-CoA dehydrogenase deficiency (VLCADD) is a hereditary disorder of mitochondrial long-chain fatty acid oxidation that manifests with variable presentations, including exercise intolerance, cardiomyopathy, and liver disease. Herein, we describe the clinical and genetic...
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| Publicado no: | Eur J Neurol |
|---|---|
| Main Authors: | , , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8006598/ https://ncbi.nlm.nih.gov/pubmed/32558070 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/ene.14402 |
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