Natural history of a mouse model of X-linked myotubular myopathy

X-linked myotubular myopathy (XLMTM) is a severe monogenetic disorder of the skeletal muscle. It is caused by loss-of-expression/function mutations in the myotubularin (MTM1) gene. Much of what is known about the disease, as well as the treatment strategies, has been uncovered through experimentatio...

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Detalles Bibliográficos
Autores principales: Sarikaya, Ege, Sabha, Nesrin, Volpatti, Jonathan, Pannia, Emanuela, Maani, Nika, Gonorazky, Hernan D., Celik, Alper, Liang, Yijng, Onofre-Oliveira, Paula, Dowling, James J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Company of Biologists Ltd 2022
Materias:
Resource Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9346535/
https://www.ncbi.nlm.nih.gov/pubmed/35694952
http://dx.doi.org/10.1242/dmm.049342

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9346535/
https://www.ncbi.nlm.nih.gov/pubmed/35694952
http://dx.doi.org/10.1242/dmm.049342

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