No causal role for the G482T and G689T polymorphisms in translation regulation of serotonin transporter (SLC6A4) or association with attention-deficit-hyperactivity disorder (ADHD)

Neuroscience Letters

Volumn 454, Issue 3, 2009, Pages 244-248

  Banerjee, Emili ^a,b   Sinha, Swagata ^b   Chatterjee, Anindita ^b   Nandagopal, Krishnadas ^a,b  

^a Manovikas Biomedical Research and Diagnostic Centre   (India)

^b Manovikas Kendra Rehabilitation and Research Institute for the Handicapped   (India)

Author keywords

ADHD; HHRR; miRNA target; Secondary structure; Serotonin transporter; TDT

Indexed keywords

MICRORNA; SEROTONIN TRANSPORTER;

3' UNTRANSLATED REGION; ALLELE; ARTICLE; ATTENTION DEFICIT DISORDER; CHILD; DISEASE ASSOCIATION; DISEASE PREDISPOSITION; FEMALE; GENE SEQUENCE; GENE TRANSLOCATION; GENETIC ASSOCIATION; GENETIC POLYMORPHISM; GENETIC VARIABILITY; GENOTYPE; HAPLOTYPE; HUMAN; INDIA; MAJOR CLINICAL STUDY; MALE; PRIORITY JOURNAL; RISK FACTOR; RNA BINDING; SCHOOL CHILD; SECONDARY ANALYSIS; STRUCTURE ANALYSIS; TRANSLATION REGULATION;

3' UNTRANSLATED REGIONS; ATTENTION DEFICIT DISORDER WITH HYPERACTIVITY; BASE SEQUENCE; CHILD; FEMALE; GENE FREQUENCY; GENETIC PREDISPOSITION TO DISEASE; HUMANS; MALE; MOLECULAR SEQUENCE DATA; POLYMERASE CHAIN REACTION; POLYMORPHISM, RESTRICTION FRAGMENT LENGTH; POLYMORPHISM, SINGLE NUCLEOTIDE; PROTEIN BIOSYNTHESIS; PROTEIN STRUCTURE, SECONDARY; RISK FACTORS; SEROTONIN PLASMA MEMBRANE TRANSPORT PROTEINS;

EID: 63449085223     PISSN: 03043940     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.neulet.2009.03.032     Document Type: Article

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