Update: More Deafness Genes
- 29 May 1998
- journal article
- other
- Published by American Association for the Advancement of Science (AAAS) in Science
- Vol. 280 (5368) , 1403
- https://doi.org/10.1126/science.280.5368.1403
Abstract
No abstract availableThis publication has 7 references indexed in Scilit:
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- Mutations in the human α-tectorin gene cause autosomal dominant non-syndromic hearing impairmentNature Genetics, 1998
- Progress in Progressive Hearing LossScience, 1998
- Nonsyndromic Deafness DFNA1 Associated with Mutation of a Human Homolog of the Drosophila Gene diaphanousScience, 1997
- The mouse Snell's waltzer deafness gene encodes an unconventional myosin required for structural integrity of inner ear hair cellsNature Genetics, 1995
- A type VII myosin encoded by the mouse deafness gene shaker-1Nature, 1995
- Pulling springs to tune transduction: Adaptation by hair cellsNeuron, 1994