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...

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Detalles Bibliográficos
Autores principales: Yang, Lan, Yang, Yang, Liu, Xingyun, Chen, Yongquan, Chen, Yalan, Lin, Yuxin, Sun, Yan, Shen, Bairong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Original Article
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

Internet

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

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