Molecular Basis of Multiple Mitochondrial Dysfunctions Syndrome 2 Caused by CYS59TYR BOLA3 Mutation

Multiple mitochondrial dysfunctions syndrome (MMDS) is a rare neurodegenerative disorder associated with mutations in genes with a vital role in the biogenesis of mitochondrial [4Fe–4S] proteins. Mutations in one of these genes encoding for BOLA3 protein lead to MMDS type 2 (MMDS2). Recently, a nove...

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Detalles Bibliográficos
Autores principales: Saudino, Giovanni, Suraci, Dafne, Nasta, Veronica, Ciofi-Baffoni, Simone, Banci, Lucia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8125686/
https://www.ncbi.nlm.nih.gov/pubmed/34063696
http://dx.doi.org/10.3390/ijms22094848

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8125686/
https://www.ncbi.nlm.nih.gov/pubmed/34063696
http://dx.doi.org/10.3390/ijms22094848

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