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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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Bibliografski detalji
Izdano u:Methods Mol Biol
Glavni autori: Chakkalakal, Salin A., Shore, Eileen M.
Format: Artigo
Jezik:Inglês
Izdano: 2019
Teme:
Online pristup: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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