Copy number variation-associated lncRNAs may contribute to the etiologies of congenital heart disease

Copy number variations (CNVs) have long been recognized as pathogenic factors for congenital heart disease (CHD). Few CHD associated CNVs could be interpreted as dosage effect due to disruption of coding sequences. Emerging evidences have highlighted the regulatory roles of long noncoding RNAs (lncR...

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Detalles Bibliográficos
Autores principales: Lu, Yibo, Fang, Qing, Qi, Ming, Li, Xiaoliang, Zhang, Xingyu, Lin, Yuwan, Xiang, Ying, Fu, Qihua, Wang, Bo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9938258/
https://www.ncbi.nlm.nih.gov/pubmed/36806749
http://dx.doi.org/10.1038/s42003-023-04565-z

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9938258/
https://www.ncbi.nlm.nih.gov/pubmed/36806749
http://dx.doi.org/10.1038/s42003-023-04565-z

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