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...

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Detalles Bibliográficos
Autores principales: Seefried, L., Banholzer, D., Fischer, R., Grafe, I., Hüning, I., Morhart, R, Oheim, R., Semler, O., Siggelkow, H., Stockklausner, C., Hoyer-Kuhn, H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Medizin 2023
Materias:
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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

Internet

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

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