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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The Company of Biologists,
2022-04-01T00:00:00Z.
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A1234.567 |
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Kopie 1 | Beschikbaar |