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Diltiazem improves contractile properties of skeletal muscle in dysferlin‐deficient BLAJ mice, but does not reduce contraction‐induced muscle damage
B6.A‐Dysf (prmd)/GeneJ (BLAJ) mice model human limb‐girdle muscular dystrophy 2B (LGMD2B), which is linked to mutations in the dysferlin (DYSF) gene. We tested the hypothesis that, the calcium ion (Ca(2+)) channel blocker diltiazem (DTZ), reduces contraction‐induced skeletal muscle damage, in BLAJ m...
Autores principales: | Begam, Morium, Collier, Alyssa F., Mueller, Amber L., Roche, Renuka, Galen, Sujay S., Roche, Joseph A. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5995314/ https://www.ncbi.nlm.nih.gov/pubmed/29890050 http://dx.doi.org/10.14814/phy2.13727 |
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Correction: Dysferlin-deficiency has greater impact on function of slow muscles, compared with fast, in aged BLAJ mice
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