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Compromised Exercise Capacity and Mitochondrial Dysfunction in the Osteogenesis Imperfecta Murine (oim) Mouse Model
Osteogenesis imperfecta (OI) is a heritable connective tissue disorder that most often arises from type I collagen, COL1A1 and COL1A2, gene defects leading to skeletal fragility, short stature, blue-gray sclera, and muscle weakness. Relative to the skeletal fragility, muscle weakness is much less un...
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| Publicado no: | J Bone Miner Res |
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| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6744299/ https://ncbi.nlm.nih.gov/pubmed/30908713 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/jbmr.3732 |
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