Neurodegenerative and functional signatures of the cerebellar cortex in m.3243A > G patients

Mutations of the mitochondrial DNA are an important cause of inherited diseases that can severely affect the tissue’s homeostasis and integrity. The m.3243A > G mutation is the most commonly observed across mitochondrial disorders and is linked to multisystemic complications, including cognitive...

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Detalles Bibliográficos
Autores principales: Haast, Roy A. M., De Coo, Irenaeus F. M., Ivanov, Dimo, Khan, Ali R., Jansen, Jacobus F. A., Smeets, Hubert J. M., Uludağ, Kâmil
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8853728/
https://www.ncbi.nlm.nih.gov/pubmed/35187487
http://dx.doi.org/10.1093/braincomms/fcac024

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8853728/
https://www.ncbi.nlm.nih.gov/pubmed/35187487
http://dx.doi.org/10.1093/braincomms/fcac024

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