Fibrodysplasia Ossificans Progressiva (FOP): A Segmental Progeroid Syndrome

Segmental progeroid syndromes are commonly represented by genetic conditions which recapitulate aspects of physiological aging by similar, disparate, or unknown mechanisms. Fibrodysplasia ossificans progressiva (FOP) is a rare genetic disease caused by mutations in the gene for ACVR1/ALK2 encoding A...

Descripción completa

Detalles Bibliográficos
Autores principales: Pignolo, Robert J., Wang, Haitao, Kaplan, Frederick S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Endocrinology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6966325/
https://www.ncbi.nlm.nih.gov/pubmed/31998237
http://dx.doi.org/10.3389/fendo.2019.00908

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6966325/
https://www.ncbi.nlm.nih.gov/pubmed/31998237
http://dx.doi.org/10.3389/fendo.2019.00908

Ejemplares similares