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Heterotopic Ossification in Mouse Models of Fibrodysplasia Ossificans Progressiva
Fibrodysplasia ossificans progressiva (FOP), a rare genetic disorder of progressive extra-skeletal ossification, is the most disabling form of heterotopic ossification (HO) in humans. Most people with FOP carry an activating mutation in a BMP type I receptor gene, ACVR1(R206H), that promotes ectopic...
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| 出版年: | Methods Mol Biol |
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| 主要な著者: | , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
2019
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7419004/ https://ncbi.nlm.nih.gov/pubmed/30414138 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/978-1-4939-8904-1_18 |
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