DNA Copy Number Variations as Markers of Mutagenic Impact

DNA copy number variation (CNV) occurs due to deletion or duplication of DNA segments resulting in a different number of copies of a specific DNA-stretch on homologous chromosomes. Implications of CNVs in evolution and development of different diseases have been demonstrated although contribution of...

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Detalles Bibliográficos
Autores principales: Hovhannisyan, Galina, Harutyunyan, Tigran, Aroutiounian, Rouben, Liehr, Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6801639/
https://www.ncbi.nlm.nih.gov/pubmed/31554154
http://dx.doi.org/10.3390/ijms20194723

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6801639/
https://www.ncbi.nlm.nih.gov/pubmed/31554154
http://dx.doi.org/10.3390/ijms20194723

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