Novel Pathogenic Variants Underlie SLC26A4-related Hearing Loss in a Multiethnic Cohort

بواسطة Cengiz, Filiz Basak, Yilmazer, Rasim, Olgun, Levent, Sennaroglu, Levent, Kirazli, Tayfun, Alper, Hudaver, Olgun, Yuksel, Incesulu, Armagan, Atik, Tahir, Hernandez, Fabiola Huesca, Domínguez-Aburto, Juan, González-Rosado, Garly, Hernandez-Zamora, Edgar, de la Luz Arenas-Sordo, Maria, Menendez, Ibis, Orhan, Kadir Serkan, Avci, Hakan, Mahdieh, Nejat, Bonyadi, Mortaza, Foster, Joseph, Duman, Duygu, Ozkinay, Ferda, Blanton, Susan H., Bademci, Guney, Tekin, Mustafa
الحاوية / القاعدة Int J Pediatr Otorhinolaryngol (2017)

Comprehensive Analysis via Exome Sequencing Uncovers Genetic Etiology in Autosomal Recessive Non-Syndromic Deafness in a Large Multiethnic Cohort

بواسطة Bademci, Guney, Foster, Joseph, Mahdieh, Nejat, Bonyadi, Mortaza, Duman, Duygu, Cengiz, F.Basak, Menendez, Ibis, Horta, Oscar Diaz, Shirkavand, Atefeh, Zeinali, Sirous, Subasioglu, Asli, Tokgoz-Yilmaz, Suna, Hernandez, Fabiola Huesca, de la Luz Arenas Sordo, Maria, Dominguez-Aburto, Juan, Hernandez-Zamora, Edgar, Montenegro, Paola, Paredes, Rosario, Moreta, Germania, Vinueza, Rodrigo, Villegas, Franklin, Mendoza Benitez, Santiago, Guo, Shengru, Bozan, Nazim, Tos, Tulay, Incesulu, Armagan, Sennaroglu, Gonca, Blanton, Susan H., Ozturkmen Akay, Hatice, Yildirim-Baylan, Muzeyyen, Tekin, Mustafa
الحاوية / القاعدة Genet Med (2015)