Ebstein’s anomaly may be caused by mutations in the sarcomere protein gene MYH7

Ebstein’s anomaly is a rare congenital heart malformation characterised by adherence of the septal and posterior leaflets of the tricuspid valve to the underlying myocardium. Associated abnormalities of left ventricular morphology and function including left ventricular noncompaction (LVNC) have bee...

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Detalles Bibliográficos
Autores principales: van Engelen, K., Postma, A. V., van de Meerakker, J. B. A., Roos-Hesselink, J. W., Helderman-van den Enden, A. T. J. M., Vliegen, H. W., Rahman, T., Baars, M. J. H., Sels, J-W, Bauer, U., Pickardt, T., Sperling, S. R., Moorman, A. F. M., Keavney, B., Goodship, J., Klaassen, S., Mulder, B. J. M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bohn Stafleu van Loghum 2011
Materias:
Review Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3578524/
https://www.ncbi.nlm.nih.gov/pubmed/21604106
http://dx.doi.org/10.1007/s12471-011-0141-1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3578524/
https://www.ncbi.nlm.nih.gov/pubmed/21604106
http://dx.doi.org/10.1007/s12471-011-0141-1

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