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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...
Gorde:
| Argitaratua izan da: | Neuropsychopharmacology |
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| Egile Nagusiak: | , , , , , , , |
| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
Nature Publishing Group
2015
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| Gaiak: | |
| Sarrera elektronikoa: | 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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