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Biochemical Assessment of Coenzyme Q(10) Deficiency
Coenzyme Q(10) (CoQ(10)) deficiency syndrome includes clinically heterogeneous mitochondrial diseases that show a variety of severe and debilitating symptoms. A multiprotein complex encoded by nuclear genes carries out CoQ(10) biosynthesis. Mutations in any of these genes are responsible for the pri...
Tallennettuna:
| Julkaisussa: | J Clin Med |
|---|---|
| Päätekijät: | , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
MDPI
2017
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5372996/ https://ncbi.nlm.nih.gov/pubmed/28273876 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/jcm6030027 |
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