Impact of copy number variations burden on coding genome in humans using integrated high resolution arrays

Copy number variations (CNVs) alter the transcriptional and translational levels of genes by disrupting the coding structure and this burden of CNVs seems to be a significant contributor to phenotypic variations. Therefore it was necessary to assess the complexities of CNV burden on the coding genom...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:Genet Res (Camb)
Egile Nagusiak: VEERAPPA, AVINASH M., LINGAIAH, KUSUMA, VISHWESWARAIAH, SANGEETHA, MURTHY, MEGHA N., SURESH, RAVIRAJ V., MANJEGOWDA, DINESH S., RAMACHANDRA, NALLUR B.
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: Cambridge University Press 2014
Gaiak:
Research Papers
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC7045015/
https://ncbi.nlm.nih.gov/pubmed/25578402
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1017/S0016672314000202
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