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When one skeleton is enough: approaches and strategies for the treatment of fibrodysplasia ossificans progressiva (FOP)
A heterozygous missense mutation in activin receptor IA/activin-like kinase-2 (ACVR1/ALK2), a bone morphogenetic protein (BMP) type I receptor, is responsible for fibrodysplasia ossificans progressiva (FOP), the most catastrophic disorder of skeletal metamorphosis in humans. The discovery of the FOP...
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| Autores principales: | , , |
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| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
2008
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3627400/ https://ncbi.nlm.nih.gov/pubmed/23599718 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ddstr.2008.11.004 |
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