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Fibrodysplasia ossificans progressiva: Basic understanding and experimental models
Fibrodysplasia ossificans progressive (FOP) is an extremely rare autosomal dominant disorder characterized by congenital malformations of the great toes and progressive heterotopic ossification that can induce a disabling second skeleton. Spontaneously occurring flare-ups can cause inflammatory soft...
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| Udgivet i: | Intractable Rare Dis Res |
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| Main Authors: | , , , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
International Research and Cooperation Association for Bio & Socio-Sciences Advancement
2017
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5735276/ https://ncbi.nlm.nih.gov/pubmed/29259851 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5582/irdr.2017.01055 |
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