Genome-Wide Association Study of Copy Number Variations (CNVs) with Opioid Dependence

Single-nucleotide polymorphisms that have been associated with opioid dependence (OD) altogether account for only a small proportion of the known heritability. Most of the genetic risk factors are unknown. Some of the ‘missing heritability' might be explained by copy number variations (CNVs) in...

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Detalhes bibliográficos
Publicado no:Neuropsychopharmacology
Main Authors: Li, Dawei, Zhao, Hongyu, Kranzler, Henry R, Li, Ming D, Jensen, Kevin P, Zayats, Tetyana, Farrer, Lindsay A, Gelernter, Joel
Formato: Artigo
Idioma:Inglês
Publicado em: Nature Publishing Group 2015
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Original Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4330517/
https://ncbi.nlm.nih.gov/pubmed/25345593
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/npp.2014.290
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