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

Genet Med 18: 364–371; advance online publication, July 30, 2015; doi:10.1038/gim.2015.89

In the published version of this manuscript in Table1: Family 7, pathogenic variant reported in TPRN as c.705_709dupCCTGC (p.R237PfsX215) is now corrected to c.701_705dupCTGCC (p.N236LfsX216); Family 52, pathogenic variant reported in TMC1 as c.1589_1590CT is now corrected to c.1589_1590delCT; Family 123, pathogenic variant in TMC1 reported as c.1080_1084delGATCA is now corrected to c.1083_1087delCAGAT, this variant has been previously reported by Kalay et al.; Family 1368, pathogenic variant in TMPRSS3 reported as c.1126G>A (p.G376S) is now corrected to c.1129G>A (p.G377S); Overall identified novel variant percentage is 53% instead of 54%. In Figure 3a, typo error for “TIME” is now corrected to “TMIE”. The authors regret the errors.

Kalay E, Karaguzel A, Caylan R, et al. Four novel TMC1 (DFNB7/DFNB11) mutations in Turkish patients with congenital autosomal recessive nonsyndromic hearing loss. Hum Mutat 2005;26:591.