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A splice-site mutation and overexpression of MY06 cause a similar phenotype in two families with autosomal dominant hearing lossHILGERT, Nele; TOPSAKAL, Vedat; VAN DINTHER, Joost et al.European journal of human genetics. 2008, Vol 16, Num 5, pp 593-602, issn 1018-4813, 10 p.Article
