The genome-wide landscape of copy number variations in the MUSGEN study provides evidence for a founder effect in the isolated Finnish population

Here we characterized the genome-wide architecture of copy number variations (CNVs) in 286 healthy, unrelated Finnish individuals belonging to the MUSGEN study, where molecular background underlying musical aptitude and related traits are studied. By using Illumina HumanOmniExpress-12v.1.0 beadchip,...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Prif Awduron: Kanduri, Chakravarthi, Ukkola-Vuoti, Liisa, Oikkonen, Jaana, Buck, Gemma, Blancher, Christine, Raijas, Pirre, Karma, Kai, Lähdesmäki, Harri, Järvelä, Irma
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: Nature Publishing Group 2013
Pynciau:
Article
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC3831076/
https://ncbi.nlm.nih.gov/pubmed/23591402
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ejhg.2013.60
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