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...

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Detalles Bibliográficos
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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2022
Materias:
Research Article
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

Internet

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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