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...

पूर्ण विवरण

में बचाया:

ग्रंथसूची विवरण
मुख्य लेखक:	Pérez-Leon, JorgeAlberto
अन्य लेखक:	Aguirre-Ramírez, Marisela, Gutiérrez-Amavizca, Bianca Ethel, Prado Montes de Oca, Ernesto, Gutiérrez-Amavizca, Jean Paul, Castro, Oscar, Ruíz-Marquez, Heriberto, Perez Conde-Andreu, Kricel, Pérez Calderón, Ricardo
स्वरूप:	Artículo
भाषा:	English
प्रकाशित:	2021
विषय:	OPN4 gene melanopsin insomnia SNPs retina chronotypes info:eu-repo/classification/cti/2
ऑनलाइन पहुंच:	https://doi.org/10.3390/ijerph18020571. https://www.mdpi.com/1660-4601/18/2/571
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