Effect of Mitochondrial and Cytosolic FXN Isoform Expression on Mitochondrial Dynamics and Metabolism

Friedreich’s ataxia (FRDA) is a neurodegenerative disease caused by recessive mutations in the frataxin gene that lead to a deficiency of the mitochondrial frataxin (FXN) protein. Alternative forms of frataxin have been described, with different cellular localization and tissue distribution, includi...

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Detalles Bibliográficos
Autores principales: Agrò, Mauro, Díaz-Nido, Javier
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7662637/
https://www.ncbi.nlm.nih.gov/pubmed/33158039
http://dx.doi.org/10.3390/ijms21218251

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7662637/
https://www.ncbi.nlm.nih.gov/pubmed/33158039
http://dx.doi.org/10.3390/ijms21218251

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