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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Detalhes bibliográficos
Publicado no:Biomed Res Int
Main Authors: 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: Artigo
Idioma:Inglês
Publicado em: Hindawi Publishing Corporation 2015
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Research Article
Acesso em linha: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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