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:
- Tipo de recurso:
- Fecha de publicación:
- 2017
- Institución:
- Universidad del Rosario
- Repositorio:
- Repositorio EdocUR - U. Rosario
- Idioma:
- eng
- OAI Identifier:
- oai:repository.urosario.edu.co:10336/26456
- Acceso en línea:
- https://doi.org/10.1017/s104795111700110x
https://repository.urosario.edu.co/handle/10336/26456
- Palabra clave:
- Cardiorespiratory Medicine and Haematology
Medical and Health Sciences
- Rights
- License
- http://purl.org/coar/access_right/c_14cb