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Autor:
Ton Schoenmaker, Michal Mokry, Dimitra Micha, Coen Netelenbos, Nathalie Bravenboer, Marjolijn Gilijamse, E. Marelise W. Eekhoff, Teun J. de Vries
Publikováno v:
Biomedicines, Vol 9, Iss 6, p 629 (2021)
Fibrodysplasia Ossificans Progressiva (FOP) is a rare genetic disease characterized by heterotopic ossification (HO). It is caused by mutations in the Activin receptor type 1 (ACVR1) gene, resulting in enhanced responsiveness to ligands, specifically
Externí odkaz:
https://doaj.org/article/cb29171e2fea443c812c34b0f05dcdad