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    • Spectrum of DNA variants for non-syndromic deafness in a large cohort from multiple continents. 

      Yan, D.; Tekin, D.; Bademci, G.; Foster, J.; Cengiz, F. B.; Kannan-Sundhari, A.; Guo, S.; Mittal, R.; Zou, B.; Grati, M.; Kabahuma, R. I.; Kameswaran, M.; Lasisi, T. J.; Adedeji, W. A.; Lasisi, A. O.; Menendez, I.; Herrera, M.; Carranza, C.; Maroofian, R.; Crosby, Andrew H.; Bensaid, M.; Masmoudi, S.; Behnam, M.; Mojarrad, M.; Feng, Y.; Duman, D.; Mawla, A. M.; Nord, A. S.; Blanton, S. H.; Liu, X. Z.; Tekin, M. (Springer, 2016-08)
      Hearing loss is the most common sensory deficit in humans with causative variants in over 140 genes. With few exceptions, however, the population-specific distribution for many of the identified variants/genes is unclear. ...