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A comparison of the bone and growth phenotype of mdx, mdx:Cmah(−/−) and mdx:Utrn(+/−) murine models with the C57BL/10 wild-type mouse
The muscular dystrophy X-linked (mdx) mouse is commonly used as a mouse model of Duchenne muscular dystrophy (DMD). Its phenotype is, however, mild, and other mouse models have been explored. The mdx:Cmah(−/−) mouse carries a human-like mutation in the Cmah gene and has a severe muscle phenotype, bu...
Tallennettuna:
| Julkaisussa: | Dis Model Mech |
|---|---|
| Päätekijät: | , , , , , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
The Company of Biologists Ltd
2020
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6994935/ https://ncbi.nlm.nih.gov/pubmed/31754018 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1242/dmm.040659 |
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