Association between a functional polymorphism in the serotonin transporter gene and diarrhoea predominant irritable bowel syndrome in women - Yeo, A; Boyd, P; Lumsden, S; Saunders, T; Handley, A; Stubbins, M; Knaggs, A; Asquith, S; Taylor, I; Bahari, B; Crocker, N; Rallan, R; et al. (Gut, 2004)
Keywords: 5-HT; 5-HTT; 5-hydroxtryptamine; 5-hydroxtryptamine transporter ( = SERT); Adolescent; Adult; Aged; Aged, 80 and over; base pair; central nervous system; cIBS; CNS; Constipation; constipation predominant irritable bowel syndrome; del; deletion; Diarrhea - genetics; diarrhoea predominant irritable bowel syndrome; dIBS; enterochromaffin (cell); Female; Genes; Genetic Predisposition to Disease; Genotype; Hardy-Weinberg equilibrium; Humans; HWE; IBS; ins; insertion; Irritable Bowel Syndrome; Irritable Bowel Syndrome - genetics; kilo base pair; linkage disequilibrium; Membrane Glycoproteins - genetics; Membrane Transport Proteins - genetics; Middle Aged; Nerve Tissue Proteins - genetics; Nervous system; PCR; Phenotype; polymerase chain reaction; polymorphism; Polymorphism, Single Nucleotide; Proteins; Rodents; Serotonin; Serotonin Plasma Membrane Transport Proteins; serotonin reuptake transporter ( = 5-HTT); serotonin transporter; SERT; single nucleotide polymorphism; SLC6A4; SNP; solute carrier family 6 member 4; Studies; variable number of tandem repeats; VNTR