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The Developmental Phenotype of the Great Toe in Fibrodysplasia Ossificans Progressiva

Fibrodysplasia ossificans progressiva (FOP) is a rare genetic disorder in which extensive heterotopic ossification (HO) begins to form during early childhood and progresses throughout life. Although HO does not occur during embryonic development, children who carry the ACVR1(R206H) mutation that cau...

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Publicat a:Front Cell Dev Biol
Autors principals: Towler, O. Will, Kaplan, Frederick S., Shore, Eileen M.
Format: Artigo
Idioma:Inglês
Publicat: Frontiers Media S.A. 2020
Matèries:
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC7753048/
https://ncbi.nlm.nih.gov/pubmed/33364240
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fcell.2020.612853
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