Duchenne's muscular dystrophy involves a defective transsulfuration pathway activity

Duchenne muscular dystrophy (DMD) is the most frequent X chromosome-linked disease caused by mutations in the gene encoding for dystrophin, leading to progressive and unstoppable degeneration of skeletal muscle tissues. Despite recent advances in the understanding of the molecular processes involved...

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Detalles Bibliográficos
Autores principales: Panza, E., Vellecco, V., Iannotti, F.A., Paris, D., Manzo, O.L., Smimmo, M., Mitilini, N., Boscaino, A., de Dominicis, G., Bucci, M., Di Lorenzo, A., Cirino, G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Research Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8246642/
https://www.ncbi.nlm.nih.gov/pubmed/34174560
http://dx.doi.org/10.1016/j.redox.2021.102040

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8246642/
https://www.ncbi.nlm.nih.gov/pubmed/34174560
http://dx.doi.org/10.1016/j.redox.2021.102040

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