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...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Julkaisussa:Biomed Res Int
Päätekijät: 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
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Hindawi Publishing Corporation 2015
Aiheet:
Research Article
Linkit: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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