Identification of genetic variants and chromosomal abnormalities associated with Ebstein anomaly
Background/Hypothesis: Ebstein Anomaly (EA) is an infrequent congenital heart defect (CHD) with considerable phenotypic heterogeneity in which right ventricle, tricuspid valve and electrical abnormalities prevail. Phenotypic diversity likely reflects an underlying genetic heterogeneity, which combin...
| Autores Principales: | , , , , , , , , , |
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| Formato: | Objeto de conferencia (Conference Object) |
| Lenguaje: | Inglés (English) |
| Publicado: |
Cambridge University Press
2017
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| Materias: | |
| Acceso en línea: | https://repository.urosario.edu.co/handle/10336/26456 https://doi.org/10.1017/s104795111700110x |