Animal Models of CMT2A: State-of-art and Therapeutic Implications

Charcot–Marie–Tooth disease type 2A (CMT2A), arising from mitofusin 2 (MFN2) gene mutations, is the most common inherited axonal neuropathy affecting motor and sensory neurons. The cellular and molecular mechanisms by which MFN2 mutations determine neuronal degeneration are largely unclear. No effec...

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Detalles Bibliográficos
Autores principales: De Gioia, Roberta, Citterio, Gaia, Abati, Elena, Nizzardo, Monica, Bresolin, Nereo, Comi, Giacomo Pietro, Corti, Stefania, Rizzo, Federica
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7541381/
https://www.ncbi.nlm.nih.gov/pubmed/32856204
http://dx.doi.org/10.1007/s12035-020-02081-3

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7541381/
https://www.ncbi.nlm.nih.gov/pubmed/32856204
http://dx.doi.org/10.1007/s12035-020-02081-3

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