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The interaction of the Chrna5 D398N variant with developmental nicotine exposure
A single nucleotide polymorphism (SNP) in CHRNA5 (rs16969968, change from an aspartic acid (D) to asparagine (N) at position 398 of the human α5 nicotinic acetylcholine receptor subunit) has been associated with increased risk for nicotine dependence. Consequently, carriers of the risk variant may b...
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| Publicado no: | Genes Brain Behav |
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| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7313682/ https://ncbi.nlm.nih.gov/pubmed/29573323 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/gbb.12474 |
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