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pro vyhledávání: '"Murtaza Bonyadi"'
Autor:
Memoona Ramzan, Duygu Duman, LeShon Chere Peart Hendricks, Shengru Guo, Ahmet Mutlu, Mahmut Tayyar Kalcioglu, Serhat Seyhan, Claudia Carranza, Murtaza Bonyadi, Nejat Mahdieh, Muzeyyen Yildirim-Baylan, Erick Figueroa-Ildefonso, Ozgul Alper, Tahir Atik, Abdurrahman Ayral, Nazim Bozan, Burhan Balta, Christian Rivas, Gabrielle N. Manzoli, Fabiola Huesca-Hernandez, Raja A. H. Kuchay, Merve Durgut, Guney Bademci, Mustafa Tekin
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 non-syndromic HL in 322 families
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7b34b9d561748a50db02b17e2cdc5635
https://hdl.handle.net/20.500.12866/13603
https://hdl.handle.net/20.500.12866/13603
Publikováno v:
Genomics & Genetics Weekly; 6/23/2023, p1230-1230, 1p
