ListarArtículos en revistas indizadas por tema "Secuenciación de Nucleótidos de Alto Rendimiento"

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Genome sequencing identifies coding and non-coding variants for non-syndromic hearing loss.

Ramzan, Memoona; Duman, Duygu; Hendricks, LeShon Chere Peart; Guo, Shengru; Mutlu, Ahmet; Kalcioglu, Mahmut Tayyar; Seyhan, Serhat; Carranza, Claudia; Bonyadi, Murtaza; Mahdieh, Nejat; Yildirim-Baylan, Muzeyyen; Figueroa Ildefonso, Erick Gianpierre; Alper, Ozgul; Atik, Tahir; Ayral, Abdurrahman; Bozan, Nazim; Balta, Burhan; Rivas, Christian; Manzoli, Gabrielle N.; Huesca-Hernandez, Fabiola; Kuchay, Raja A. H.; Durgut, Merve; Bademci, Guney; Tekin, Mustafa (Springer, 2023)

Hearing loss (HL) is a common heterogeneous trait that involves variants in more than 200 genes. In this study, we utilized exome (ES) and genome sequencing (GS) to effectively identify the genetic cause of presumably ...

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