PuSH - Publication Server of Helmholtz Zentrum München

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1.
Weegerink, N.J.* et al.: Genotype-phenotype correlation in DFNB8/10 families with TMPRSS3 mutations. J. Assoc. Res. Otolaryngol. 12, 756-766 (2011)
2.
Collin, R.W.* et al.: Mid-frequency DFNA8/12 hearing loss caused by a synonymous TECTA mutation that affects an exonic splice enhancer. Eur. J. Hum. Genet. 16, 1430-1436 (2008)