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per3 protein, human
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The PER3rs772027021 SNP induces pigmentation phenotypes of dyschromatosis universalis hereditaria.
PERIOD3 (PER3) VNTR Variant Associated with Seasonal Pattern and Family History in Bipolar Disorder.
Evaluation of a circadian rhythm gene (PER3) VNTR variant in Turkish athletes.
Dim light melatonin onset following simulated eastward travel is earlier in young males genotyped as…
Moderating effects of PER3 gene DNA methylation on the association of sleep quality with mental heal…
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Chronotype of Patients With Type 2 Diabetes and Effect on Glycaemic Control
Exogenous Melatonin in Intensive Care Unit Chronodisruption
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