Genetic variation in melatonin pathway enzymes in children with autism spectrum disorder and comorbid sleep onset delay.

Veatch OJ, Pendergast JS, Allen MJ, Leu RM, Johnson CH, Elsea SH, Malow BA
J Autism Dev Disord. 2015 45 (1): 100-10

PMID: 25059483 · PMCID: PMC4289108 · DOI:10.1007/s10803-014-2197-4

MeSH Terms (15)

Acetylserotonin O-Methyltransferase Child Child, Preschool Child Development Disorders, Pervasive Clinical Trials as Topic Cytochrome P-450 CYP1A2 DNA Mutational Analysis Endophenotypes Genotype Humans Male Melatonin Mutation Polymorphism, Single Nucleotide Sleep Initiation and Maintenance Disorders

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