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CHDGKB: a knowledgebase for systematic understanding of genetic variations associated with non-syndromic congenital heart disease
Congenital heart disease (CHD) is one of the most common birth defects, with complex genetic and environmental etiologies. The reports of genetic variation associated with CHD have increased dramatically in recent years due to the revolutionary development of molecular technology. However, CHD is a...
| Autores principales: | , , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Oxford University Press
2020
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7327432/ https://www.ncbi.nlm.nih.gov/pubmed/32608479 http://dx.doi.org/10.1093/database/baaa048 |