The mouse Ames waltzer hearing-loss mutant is caused by mutation of Pcdh15, a novel protocadherin gene
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics
Link
http://www.nature.com/articles/ng0101_99.pdf
Reference19 articles.
1. Kalatzis, V. & Petit, C. The fundamental and medical impacts of recent progress in research on hereditary hearing loss. Hum. Mol. Genet. 7, 1589–1597 (1998).
2. Corwin, J.T. Identifying the genes of hearing, deafness, and disequilibrium. Proc. Natl. Acad. Sci. USA 95, 12080– 12082 (1998).
3. Willems, P.J. Mechanism of disease: genetic causes of hearing loss. N. Engl. J. Med. 342, 1101–1109 ( 2000).
4. Osako, S. & Hilding, D.A. Electron microscopic studies of capillary permeability in normal and Ames Waltzer deaf mice. Acta Otolaryngol. 71, 365–376 (1971).
5. Alagramam, K.N. et al. A new mouse insertional mutation that causes sensorineural deafness and vestibular defects. Genetics 152, 1691–1699 (1999).
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