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

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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Main Authors: Rafael Herrera-Esparza, Deyanira Pacheco-Tovar, Juan José Bollain-y-Goytia, Felipe Torres del Muro, Roxana Ramírez-Sandoval, María Guadalupe Pacheco-Tovar, María Castañeda-Ureña, Esperanza Avalos-Díaz
Format: Article
Language:English
Published: Wiley 2013-01-01
Series:Case Reports in Genetics
Online Access:http://dx.doi.org/10.1155/2013/260371
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http://dx.doi.org/10.1155/2013/260371

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