Genetic variants in melatonin synthesis and signaling pathway are not associated with adolescent idiopathic scoliosis - Nelson, Lesa M; Ward, Kenneth; Ogilvie, James W (Spine (Philadelphia, Pa. 1976), 2011)
Keywords: Acetylserotonin O-Methyltransferase - genetics; Adolescent; Arylalkylamine N-Acetyltransferase - genetics; Case-Control Studies; Chi-Square Distribution; Gene Frequency; Genetic Association Studies; Genetic Predisposition to Disease; High-Throughput Nucleotide Sequencing; Humans; Melatonin - biosynthesis; Melatonin - genetics; Melatonin - metabolism; Odds Ratio; Oligonucleotide Array Sequence Analysis; Phenotype; Polymorphism, Single Nucleotide; Protein Kinase C-delta - genetics; Radiography; Receptor, Melatonin, MT1 - genetics; Risk Assessment; Risk Factors; Scoliosis - diagnostic imaging; Scoliosis - genetics; Scoliosis - metabolism; Signal Transduction - genetics; Tryptophan Hydroxylase - genetics; United States