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The impact of Mendelian sleep and circadian genetic variants in a population setting
Rare variants in ten genes have been reported to cause Mendelian sleep conditions characterised by extreme sleep duration or timing. These include familial natural short sleep (ADRB1, DEC2/BHLHE41, GRM1 and NPSR1), advanced sleep phase (PER2, PER3, CRY2, CSNK1D and TIMELESS) and delayed sleep phase...
Autores principales: | Weedon, Michael N., Jones, Samuel E., Lane, Jacqueline M., Lee, Jiwon, Ollila, Hanna M., Dawes, Amy, Tyrrell, Jess, Beaumont, Robin N., Partonen, Timo, Merikanto, Ilona, Rich, Stephen S., Rotter, Jerome I., Frayling, Timothy M., Rutter, Martin K., Redline, Susan, Sofer, Tamar, Saxena, Richa, Wood, Andrew R. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9499244/ https://www.ncbi.nlm.nih.gov/pubmed/36137075 http://dx.doi.org/10.1371/journal.pgen.1010356 |
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