Extensive genic and allelic heterogeneity underlying inherited retinal dystrophies in Mexican patients molecularly analyzed by next-generation sequencing.
Juan Carlos Zenteno RuizLeopoldo A García-MontañoMarisa Cruz-AguilarJosué RonquilloAgustín Rodas-SerranoLuis Aguilar-CastulRodrigo MatsuiCarlos I Vencedor-MerazRocío Arce-GonzálezFederico Graue-WiechersMario Gutiérrez-PazTatiana Urrea-VictoriaUlises de Dios CuadrasOscar F Chacón-CamachoPublished in: Molecular genetics & genomic medicine (2019)
Our results illustrate the utility of NGS for genetic diagnosis of RDs of different populations for a better knowledge of the mutational landscape associated with the disease.