The role of DNA methylation in syndromic and non-syndromic congenital heart disease

Congenital heart disease (CHD) is a common structural birth defect worldwide, and defects typically occur in the walls and valves of the heart or enlarged blood vessels. Chromosomal abnormalities and genetic mutations only account for a small portion of the pathogenic mechanisms of CHD, and the etio...

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Detalles Bibliográficos
Autores principales: Cao, Jiali, Wu, Qichang, Huang, Yanru, Wang, Lingye, Su, Zhiying, Ye, Huiming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8077695/
https://www.ncbi.nlm.nih.gov/pubmed/33902696
http://dx.doi.org/10.1186/s13148-021-01077-7

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8077695/
https://www.ncbi.nlm.nih.gov/pubmed/33902696
http://dx.doi.org/10.1186/s13148-021-01077-7

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