A Novel MYO6 Splice Site Mutation Causes Autosomal Dominant Sensorineural Hearing Loss Type DFNA22 with a Favourable Outcome after Cochlear Implantation
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R. Lang-Roth | D. Beutner | C. Kubisch | G. Borck | A. Volk | G. Nuernberg | P. Nuernberg | Gökhan Yigit | Stephan Rosenkranz