Genetic variation in melatonin pathway enzymes in children with autism spectrum disorder and comorbid sleep onset delay. [electronic resource]
Producer: 20150810Description: 100-10 p. digitalISSN:- 1573-3432
- Acetylserotonin O-Methyltransferase -- genetics
- Child
- Child Development Disorders, Pervasive -- complications
- Child, Preschool
- Clinical Trials as Topic
- Cytochrome P-450 CYP1A2 -- genetics
- DNA Mutational Analysis
- Endophenotypes
- Genotype
- Humans
- Male
- Melatonin -- biosynthesis
- Mutation -- genetics
- Polymorphism, Single Nucleotide -- genetics
- Sleep Initiation and Maintenance Disorders -- complications
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Publication Type: Journal Article; Research Support, N.I.H., Extramural
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