A Reassessment of Copy Number Variations in Congenital Heart Defects: Picturing the Whole Genome

Copy number variations (CNVs) can modulate phenotypes by affecting protein-coding sequences directly or through interference of gene expression. Recent studies in cancer and limb defects pinpointed the relevance of non-coding gene regulatory elements such as long non-coding RNAs (lncRNAs) and topolo...

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Detalles Bibliográficos
Autores principales: Meerschaut, Ilse, Vergult, Sarah, Dheedene, Annelies, Menten, Björn, De Groote, Katya, De Wilde, Hans, Muiño Mosquera, Laura, Panzer, Joseph, Vandekerckhove, Kristof, Coucke, Paul J., De Wolf, Daniël, Callewaert, Bert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8304049/
https://www.ncbi.nlm.nih.gov/pubmed/34356064
http://dx.doi.org/10.3390/genes12071048

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8304049/
https://www.ncbi.nlm.nih.gov/pubmed/34356064
http://dx.doi.org/10.3390/genes12071048

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