In the January/February 2011 issue of Genetic Testing and Molecular Biomarkers (Volume 15, Number 1-2, pp. 29-33), the article ‘‘Screening of 38 Genes Identifies Mutations in 62% of Families with Nonsyndromic Deafness in Turkey ’’ by Duygu Duman et al., in Table 1 the mutation name for family 550 was originally printed as c.5710-1G>A and should be NM_016239.3:c.5650-1G>A (myosin XVa); for family 681 the mutation name was originally printed as c.5122_5123ins20 (p.T1708KfsX9) and should be NM_022124.5: c.5122_5123insAAGTCAGCCACGGCCGCTACA (cadherin-related 23, transcript variant 1) as well as NP_071407.4: p.Tyr1707_Thr1708insLysValSerHisGlyArgTyr (cadherin-23 isoform 1).

The authors regret the error.