Reduced climbing and increased slipping adaptation in cochlear hair cells of mice with Myo7a mutations
Author:
Publisher
Springer Science and Business Media LLC
Subject
General Neuroscience
Link
http://www.nature.com/articles/nn784.pdf
Reference47 articles.
1. Gibson, F. et al. A type VII myosin encoded by the mouse deafness gene shaker-1. Nature 374, 62–64 (1995).
2. Weil, D. et al. Defective myosin VIIA gene responsible for Usher syndrome type 1B. Nature 374, 60–61 (1995).
3. Liu, X. Z. et al. Mutations in the myosin VIIA gene cause non-syndromic recessive deafness. Nat. Genet. 16, 188–190 (1997).
4. Weil, D. et al. The autosomal recessive isolated deafness, DFNB2, and the Usher 1B syndrome are allelic defects of the myosin-VIIA gene. Nat. Genet. 16, 191–193 (1997).
5. Lord, E. M. & Gates, W. H. Shaker, a new mutation of the house mouse (Mus musculus). Am. Nat. 63, 435–442 (1929).
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