Associated Papers
Melatonin receptor 1A variants as genetic cause of idiopathic osteoporosis.
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Science Translational Medicine, 2024
Identification of Key Regions Mediating Human Melatonin Type 1 Receptor Functional Selectivity Revealed by Natural Variants.
Hegron A et al.
Acs Pharmacology & Translational Science, 2021
De novo mutations in moderate or severe intellectual disability.
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25356899 (PubMed )
Supplement: pgen.1004772.s004.xlsx › 1883.659
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