Two deaf mice, two deaf mice...

1. Vahava, O. et al. Mutation in transcription factor POU4F3 associated with inherited progressive hearing loss in humans. Science 279, 1950−1953 (1998). | Article | PubMed  | ISI | ChemPort |
2. Verhoeven, K. et al. Mutations in human -tectorin cause autosomal dominant non-syndromic hearing loss (DFNA8/DFNA12). Nature Genet. 19, 60−62 (1998). | PubMed  | ISI | ChemPort |
3. Erkman, L. et al. Role of transcription factors Brn-3.1 and Brn-3.2 in auditory and visual system development. Nature 381, 603−606 (1996). | Article | PubMed  | ISI | ChemPort |
4. Lynch, E.D. et al. Nonsyndromic deafness DFNA1 associated with mutation of a human homolog of the Drosophila gene diaphanous. Science 278, 1315−1318 (1997). | Article | PubMed  | ISI | ChemPort |
5. Van Camp, G., Willems, P.J. & Smith, R.J.H. Nonsyndromic hearing impairment: unparalleled heterogeneity. Am. J. Hum. Genet. 60, 758−764 (1997). | PubMed  | ChemPort |
6. Van Camp, G. & Smith, R.J.H. Hereditary hearing loss homepage. World Wide Web URL: http://dnalab-www.uia.ac.be/dnalab/hhh/ (1998).
7. Steel, K.P. Inherited hearing defects in mice. Annu. Rev. Genet. 29, 675−701 (1995). | Article | PubMed  | ISI | ChemPort |
8. Nicolson, T. et al. Genetic analysis of vertebrate sensory hair cell mechanosensation: the zebrafish circler mutants. Neuron 20, 271−283 (1998). | Article | PubMed  | ISI | ChemPort |

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