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

• Hoofdauteurs: Johann Böhm (Auteur), Inès Barthélémy (Auteur), Charlène Landwerlin (Auteur), Nicolas Blanchard-Gutton (Auteur), Frédéric Relaix (Auteur), Stéphane Blot (Auteur), Jocelyn Laporte (Auteur), Laurent Tiret (Auteur)
• Formaat: Boek
• Gepubliceerd in: The Company of Biologists, 2022-04-01T00:00:00Z.
• Onderwerpen: article
• Online toegang: Connect to this object online.

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...