Congenital Heart Diseases: Genetic Risk Variants and Their Methylation Status

(1) Background: The interaction between single nucleotide variants (SNVs) associated with congenital heart diseases (CHDs) and their gene methylation status has not been well researched. The aim of the present study was to determine if there is a relationship between the methy lation status (MS) of...

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Detalles Bibliográficos
Autores principales: Calzada-Dávila, Melissa, Calvo-Anguiano, Geovana, Martínez-de-Villarreal, Laura E., Lugo-Trampe, José J., González-Peña, Sandra M., Ancer-Rodríguez, Patricia R., Hernández-Almaguer, María D., Campos-Acevedo, Luis D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9690480/
https://www.ncbi.nlm.nih.gov/pubmed/36421790
http://dx.doi.org/10.3390/genes13112115

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9690480/
https://www.ncbi.nlm.nih.gov/pubmed/36421790
http://dx.doi.org/10.3390/genes13112115

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