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...

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Detalles Bibliográficos
Autores principales: Rodríguez-Aguilera, Juan Carlos, Cortés, Ana Belén, Fernández-Ayala, Daniel J. M., Navas, Plácido
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5372996/
https://www.ncbi.nlm.nih.gov/pubmed/28273876
http://dx.doi.org/10.3390/jcm6030027

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5372996/
https://www.ncbi.nlm.nih.gov/pubmed/28273876
http://dx.doi.org/10.3390/jcm6030027

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