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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Vydáno v:Biomed Res Int
Hlavní autoři: 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
Médium: Artigo
Jazyk:Inglês
Vydáno: Hindawi Publishing Corporation 2015
Témata:
Research Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC4365367/
https://ncbi.nlm.nih.gov/pubmed/25834824
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2015/718786
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