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,...

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Main Authors: Kanduri, Chakravarthi, Ukkola-Vuoti, Liisa, Oikkonen, Jaana, Buck, Gemma, Blancher, Christine, Raijas, Pirre, Karma, Kai, Lähdesmäki, Harri, Järvelä, Irma
Formato: Artigo
Idioma:Inglês
Publicado: Nature Publishing Group 2013
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Article
Acceso en liña: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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