Veatch, Olivia J <br/><br/>
Genetic variation in melatonin pathway enzymes in children with autism spectrum disorder and comorbid sleep onset delay.  [electronic resource] 

 -  Journal of autism and developmental disorders  Jan 2015 
 - 100-10 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, N.I.H., Extramural 
<br/><br/><label>ISSN: </label>1573-3432 
<br/><br/><label>Standard No.: </label>10.1007/s10803-014-2197-4  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Acetylserotonin O-Methyltransferase--genetics<br/>Child<br/>Child Development Disorders, Pervasive--complications<br/>Child, Preschool<br/>Clinical Trials as Topic<br/>Cytochrome P-450 CYP1A2--genetics<br/>DNA Mutational Analysis<br/>Endophenotypes<br/>Genotype<br/>Humans<br/>Male<br/>Melatonin--biosynthesis<br/>Mutation--genetics<br/>Polymorphism, Single Nucleotide--genetics<br/>Sleep Initiation and Maintenance Disorders--complications