A genetic association study of single nucleotide polymorphisms in GNβ3 and COMT in elderly patients with irritable bowel syndrome

BACKGROUND: Several polymorphisms have been reported to be associated with irritable bowel syndrome (IBS), including C825T, the single nucleotide polymorphism (SNP), responsible for a truncated G protein β3 subunit (GNβ3), and the Vall158Met substitution in catechol-O-methyltransferase (COMT). We in...

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Detalles Bibliográficos
Autores principales: Wang, Yuezhi, Wu, Zhengyu, Qiao, Hui, Zhang, Yu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scientific Literature, Inc. 2014
Materias:
Clinical Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4113520/
https://www.ncbi.nlm.nih.gov/pubmed/25037115
http://dx.doi.org/10.12659/MSM.890315

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4113520/
https://www.ncbi.nlm.nih.gov/pubmed/25037115
http://dx.doi.org/10.12659/MSM.890315

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