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Empfehlungen zur Versorgung von Patient:innen mit FOP
BACKGROUND: Fibrodysplasia ossificans progressiva (FOP) is a very rare, severe genetic disorder triggered by a gain-of-function mutation in the ACVR1 gene that codes for the type I bone morphogenetic protein (BMP) receptor ACVR1 (activin A receptor—type 1), also known as ALK2 (activin receptor-like...
| Autores principales: | , , , , , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Springer Medizin
2023
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10622346/ https://www.ncbi.nlm.nih.gov/pubmed/37603129 http://dx.doi.org/10.1007/s00132-023-04425-y |