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BMP type I receptor inhibition reduces heterotopic ossification
Fibrodysplasia ossificans progressiva (FOP) is a congenital disorder of progressive and widespread postnatal ossification of soft tissues1–4 and is without known effective treatments. Affected individuals harbor conserved mutations in the ACVR1 gene that are thought to cause constitutive activation...
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| Main Authors: | , , , , , , , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
2008
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2846458/ https://ncbi.nlm.nih.gov/pubmed/19029982 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/nm.1888 |
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