Cardiac Alpha-Myosin (MYH6) Is the Predominant Sarcomeric Disease Gene for Familial Atrial Septal Defects

Secundum-type atrial septal defects (ASDII) account for approximately 10% of all congenital heart defects (CHD) and are associated with a familial risk. Mutations in transcription factors represent a genetic source for ASDII. Yet, little is known about the role of mutations in sarcomeric genes in AS...

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Detalles Bibliográficos
Autores principales: Posch, Maximilian G., Waldmuller, Stephan, Müller, Melanie, Scheffold, Thomas, Fournier, David, Andrade-Navarro, Miguel A., De Geeter, Bernard, Guillaumont, Sophie, Dauphin, Claire, Yousseff, Dany, Schmitt, Katharina R., Perrot, Andreas, Berger, Felix, Hetzer, Roland, Bouvagnet, Patrice, Özcelik, Cemil
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3237499/
https://www.ncbi.nlm.nih.gov/pubmed/22194935
http://dx.doi.org/10.1371/journal.pone.0028872

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3237499/
https://www.ncbi.nlm.nih.gov/pubmed/22194935
http://dx.doi.org/10.1371/journal.pone.0028872

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