Author:
Liu Xue-Zhong,Walsh James,Mburu Philomena,Kendrick-Jones John,Cope M. Jamie T.V.,Steel Karen P.,Brown Steve D.M.
Publisher
Springer Science and Business Media LLC
Reference19 articles.
1. Fraser, G.R., Causes of Profound Deafness in Childhood. (Johns Hopkins University Press, Baltimore, 1976).
2. Kelsell, D.P. et al. Connexin 26 mutations in hereditary non-syndromic sensorineural deafness. Nature 387, 80–82.
3. Steel, K.P. & Brown, S.D.M. Genetics of deafness. Curr. Opin. in Neurobiol. 6, 520–525 (1996).
4. Guilford, P. et al. A human gene responsible for neurosensory, non-syndromic recessive deafness is a candidate homologue of the mouse sh1 gene. Hum. Mol. Genet. 3, 989–993 (1994).
5. Gibson, F. et al. A type VII myosin encoded by the mouse deafness gene shaker-1. Nature 374, 62–64 (1995).
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