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Rare missense variants in CHRNB4 are associated with reduced risk of nicotine dependence
Genome-wide association studies have identified common variation in the CHRNA5–CHRNA3–CHRNB4 and CHRNA6–CHRNB3 gene clusters that contribute to nicotine dependence. However, the role of rare variation in risk for nicotine dependence in these nicotinic receptor genes has not been studied. We undertoo...
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| Main Authors: | , , , , , , , , , , , , |
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| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
Oxford University Press
2012
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| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3259016/ https://ncbi.nlm.nih.gov/pubmed/22042774 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddr498 |
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