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Novel Mutations in the Transcriptional Activator Domain of the Human TBX20 in Patients with Atrial Septal Defect

Background. The relevance of TBX20 gene in heart development has been demonstrated in many animal models, but there are few works that try to elucidate the effect of TBX20 mutations in human congenital heart diseases. In these studies, all missense mutations associated with atrial septal defect (ASD...

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Detalles Bibliográficos
Autores principales: Monroy-Muñoz, Irma Eloisa, Pérez-Hernández, Nonanzit, Rodríguez-Pérez, José Manuel, Muñoz-Medina, José Esteban, Angeles-Martínez, Javier, García-Trejo, José J., Morales-Ríos, Edgar, Massó, Felipe, Sandoval-Jones, Juan Pablo, Cervantes-Salazar, Jorge, García-Montes, José Antonio, Calderón-Colmenero, Juan, Vargas-Alarcón, Gilberto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4365367/
https://www.ncbi.nlm.nih.gov/pubmed/25834824
http://dx.doi.org/10.1155/2015/718786