Genome sequencing identifies coding and non-coding variants for non-syndromic hearing loss
Memoona Ramzan, Duygu Duman, LeShon Chere Peart Hendricks, Shengru Guo, Ahmet Mutlu, M. Tayyar Kalcıoğlu, Serhat Seyhan, Claudia Carranza, Murtaza Bonyadi, Nejat Mahdieh, Muzeyyen Yildirim‐Baylan, Erick Figueroa-Ildefonso, Özgül M. Alper, Tahir Atık, Abdurrahman Ayral, Nazım Bozan, Burhan Balta, Christian Rivas, Gabrielle Novais Manzoli, Fabiola Huesca-Hernández, Raja A. H. Kuchay, Merve Durgut, Güney Bademci, Mustafa Tekin
Topics & Concepts
GeneticsProbandExome sequencingBiologyMissense mutationFrameshift mutationGeneExomeGenomePhenotypeMutationHearing, Cochlea, Tinnitus, GeneticsEar Surgery and Otitis MediaConnexins and lens biology