Variations in Multiple Syndromic Deafness Genes Mimic Non-syndromic Hearing Loss

Author:

Bademci G.,Cengiz F. B.,Foster II J.,Duman D.,Sennaroglu L.,Diaz-Horta O.,Atik T.,Kirazli T.,Olgun L.,Alper H.,Menendez I.,Loclar I.,Sennaroglu G.,Tokgoz-Yilmaz S.,Guo S.,Olgun Y.,Mahdieh N.,Bonyadi M.,Bozan N.,Ayral A.,Ozkinay F.,Yildirim-Baylan M.,Blanton S. H.,Tekin M.

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

Reference60 articles.

1. Morton, C. C. & Nance, W. E. Newborn hearing screening–a silent revolution. N Engl J Med 354, 2151–2164 (2006).

2. Van Camp, G., Willems, P. J. & Smith, R. J. Nonsyndromic hearing impairment: unparalleled heterogeneity. Am J Hum Genet 60, 758–764 (1997).

3. http://hereditaryhearingloss.org/ .

4. Toriello et al. Hereditary Hearing Loss and Its Syndromes. Oxford University Press (2013).

5. Khan, M. R., Bashir, R. & Naz, S. SLC26A4 mutations in patients with moderate to severe hearing loss. Biochem Genet 51, 514–523 (2013).

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