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• W2069178669 abstract "Advances in the molecular biology of hearing and deafness have identified many genes essential for normal auditory function. Allele variants of these genes cause nonsyndromic deafness, making mutation screening a valuable test to unequivocally diagnose many different forms of inherited deafness. In this study, genetic testing of GJB2, SLC26A4 and WFS1 is reviewed. © 2004 Wiley-Liss, Inc." @default.
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• W2069178669 date "2004-01-01" @default.
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• W2069178669 title "Clinical application of genetic testing for deafness" @default.
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• W2069178669 doi "https://doi.org/10.1002/ajmg.a.30053" @default.
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