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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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Publicat a:Genes Brain Behav
Autors principals: O’Neill, Heidi C., Wageman, Charles R., Sherman, Sarah E., Grady, Sharon R., Marks, Michael J., Stitzel, Jerry A.
Format: Artigo
Idioma:Inglês
Publicat: 2018
Matèries:
Accés en línia: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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