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Mitochondrial Fatty Acid Oxidation Disorders: Laboratory Diagnosis, Pathogenesis, and the Complicated Route to Treatment
Mitochondrial fatty acid (FA) oxidation deficiencies represent a genetically heterogeneous group of diseases in humans caused by defects in mitochondrial FA beta-oxidation (mFAO). A general characteristic of all mFAO disorders is hypoketotic hypoglycemia resulting from the enhanced reliance on gluco...
Αποθηκεύτηκε σε:
| Τόπος έκδοσης: | J Lipid Atheroscler |
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| Κύριοι συγγραφείς: | , , , , |
| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
Korean Society of Lipidology and Atherosclerosis
2020
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| Θέματα: | |
| Διαθέσιμο Online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7521971/ https://ncbi.nlm.nih.gov/pubmed/33024728 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.12997/jla.2020.9.3.313 |
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