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...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Haller, Gabe, Druley, Todd, Vallania, Francesco L., Mitra, Robi D., Li, Ping, Akk, Gustav, Steinbach, Joe Henry, Breslau, Naomi, Johnson, Eric, Hatsukami, Dorothy, Stitzel, Jerry, Bierut, Laura J., Goate, Alison M.
Formato: Artigo
Lenguaje:Inglês
Publicado: Oxford University Press 2012
Materias:
Articles
Acceso en línea: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
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!

Ejemplares similares