Fibrodysplasia Ossificans Progressiva: What Have We Achieved and Where Are We Now? Follow-up to the 2015 Lorentz Workshop

Fibrodysplasia ossificans progressiva (FOP) is an ultra-rare progressive genetic disease effecting one in a million individuals. During their life, patients with FOP progressively develop bone in the soft tissues resulting in increasing immobility and early death. A mutation in the ACVR1 gene was id...

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Detalles Bibliográficos
Autores principales: de Ruiter, Ruben D., Smilde, Bernard J., Pals, Gerard, Bravenboer, Nathalie, Knaus, Petra, Schoenmaker, Ton, Botman, Esmée, Sánchez-Duffhues, Gonzalo, Pacifici, Maurizio, Pignolo, Robert J., Shore, Eileen M., van Egmond, Marjolein, Van Oosterwyck, Hans, Kaplan, Frederick S., Hsiao, Edward C., Yu, Paul B., Bocciardi, Renata, De Cunto, Carmen Laura, Longo Ribeiro Delai, Patricia, de Vries, Teun J., Hilderbrandt, Susanne, Jaspers, Richard T., Keen, Richard, Koolwijk, Peter, Morhart, Rolf, Netelenbos, Jan C., Rustemeyer, Thomas, Scott, Christiaan, Stockklausner, Clemens, ten Dijke, Peter, Triffit, James, Ventura, Francesc, Ravazzolo, Roberto, Micha, Dimitra, Eekhoff, Elisabeth M. W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Endocrinology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8631510/
https://www.ncbi.nlm.nih.gov/pubmed/34858325
http://dx.doi.org/10.3389/fendo.2021.732728

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8631510/
https://www.ncbi.nlm.nih.gov/pubmed/34858325
http://dx.doi.org/10.3389/fendo.2021.732728

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