The Effect of Methylmalonic Acid Treatment on Human Neuronal Cell Coenzyme Q(10) Status and Mitochondrial Function

Methylmalonic acidemia is an inborn metabolic disease of propionate catabolism, biochemically characterized by accumulation of methylmalonic acid (MMA) to millimolar concentrations in tissues and body fluids. However, MMA’s role in the pathophysiology of the disorder and its status as a “toxic inter...

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Detalles Bibliográficos
Autores principales: Proctor, Emma C., Turton, Nadia, Boan, Elle Jo, Bennett, Emily, Philips, Suzannah, Heaton, Robert A., Hargreaves, Iain P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Communication
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7730949/
https://www.ncbi.nlm.nih.gov/pubmed/33266298
http://dx.doi.org/10.3390/ijms21239137

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7730949/
https://www.ncbi.nlm.nih.gov/pubmed/33266298
http://dx.doi.org/10.3390/ijms21239137

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