Identifying missing pieces in color vision defects: a genome-wide association study in Silk Road populations

Introduction: Color vision defects (CVDs) are conditions characterized by the alteration of normal trichromatic vision. CVDs can arise as the result of alterations in three genes (OPN1LW, OPN1MW, OPN1SW) or as a combination of genetic predisposition and environmental factors. To date, apart from Men...

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Detalles Bibliográficos
Autores principales: Nardone, Giuseppe Giovanni, Spedicati, Beatrice, Concas, Maria Pina, Santin, Aurora, Morgan, Anna, Mazzetto, Lorenzo, Battaglia-Parodi, Maurizio, Girotto, Giorgia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10288324/
https://www.ncbi.nlm.nih.gov/pubmed/37359372
http://dx.doi.org/10.3389/fgene.2023.1161696

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10288324/
https://www.ncbi.nlm.nih.gov/pubmed/37359372
http://dx.doi.org/10.3389/fgene.2023.1161696

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