Copy number variations and their effect on the plasma proteome

Structural variations, including copy number variations (CNVs), affect around 20 million bases in the human genome and are common causes of rare conditions. CNVs are rarely investigated in complex disease research because most CNVs are not targeted on the genotyping arrays or the reference panels fo...

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Detalles Bibliográficos
Autores principales: Schmitz, Daniel, Li, Zhiwei, Lo Faro, Valeria, Rask-Andersen, Mathias, Ameur, Adam, Rafati, Nima, Johansson, Åsa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Investigation
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10697815/
https://www.ncbi.nlm.nih.gov/pubmed/37793096
http://dx.doi.org/10.1093/genetics/iyad179

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10697815/
https://www.ncbi.nlm.nih.gov/pubmed/37793096
http://dx.doi.org/10.1093/genetics/iyad179

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