A dog model for centronuclear myopathy carrying the most common DNM2 mutation

Mutations in DNM2 cause autosomal dominant centronuclear myopathy (ADCNM), a rare disease characterized by skeletal muscle weakness and structural anomalies of the myofibres, including nuclear centralization and mitochondrial mispositioning. Following the clinical report of a Border Collie male with...

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Detalles Bibliográficos
Autores principales: Böhm, Johann, Barthélémy, Inès, Landwerlin, Charlène, Blanchard-Gutton, Nicolas, Relaix, Frédéric, Blot, Stéphane, Laporte, Jocelyn, Tiret, Laurent
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/PMC9016898/
https://www.ncbi.nlm.nih.gov/pubmed/35244154
http://dx.doi.org/10.1242/dmm.049219

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9016898/
https://www.ncbi.nlm.nih.gov/pubmed/35244154
http://dx.doi.org/10.1242/dmm.049219

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