Association of P10L Polymorphism in Melanopsin Gene with Chronic Insomnia in Mexicans

Association of P10L Polymorphism in Melanopsin Gene with Chronic Insomnia in Mexicans

The aim of this pilot study was to determine the association of the P10L (rs2675703) polymorphism of the OPN4 gene with chronic insomnia in uncertain etiology in a Mexican population. A case control study was performed including 98 healthy subjects and 29 individuals with chronic insomnia not relate...

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其他作者:	Gutiérrez-Amavizca, Bianca Ethel, Aguirre-Ramírez, Marisela, Pérez-Leon, JorgeAlberto, Prado Montes de Oca, Ernesto, Gutiérrez-Amavizca, Jaime Paul, Castro, Oscar David, Ruíz-Marquez, Cesar Heriberto, Perez Conde-Andreu, Kricel, Pérez Calderón, Ricardo
格式:	Artículo
语言:	English
出版:	2021
主题:	OPN4 gene insomnia SNPs retina chronotypes info:eu-repo/classification/cti/2
在线阅读:	https://doi.org/10.3390/ ijerph18020571 https://www.mdpi.com/1660-4601/18/2/571
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