An Activin Receptor IA/Activin-Like Kinase-2 (R206H) Mutation in Fibrodysplasia Ossificans Progressiva

Fibrodysplasia ossificans progressiva (FOP) is an exceptionally rare genetic disease that is characterised by congenital malformations of the great toes and progressive heterotopic ossification (HO) in specific anatomical areas. This disease is caused by a mutation in activin receptor IA/activin-lik...

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Detalhes bibliográficos
Main Authors: Herrera-Esparza, Rafael, Pacheco-Tovar, Deyanira, Bollain-y-Goytia, Juan José, Torres del Muro, Felipe, Ramírez-Sandoval, Roxana, Pacheco-Tovar, María Guadalupe, Castañeda-Ureña, María, Avalos-Díaz, Esperanza
Formato: Artigo
Idioma:Inglês
Publicado em: Hindawi Publishing Corporation 2013
Assuntos:
Case Report
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3638569/
https://ncbi.nlm.nih.gov/pubmed/23653868
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2013/260371
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