A new spontaneous mutation in the mouse protocadherin 15 gene von Zheng, Q.Y., Yu, H., Washington, J.L., Kisley, L.B., Kikkawa, Y.S., Pawlowski, K.S., Wright, C.G., Alagramam, K.N.

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Neuroepithelial defects of the inner ear in a new allele of the mouse mutation Ames waltzer von Alagramam, K.N., Zahorsky-Reeves, J., Wright, C.G., Pawlowski, K.S., Erway, L.C., Stubbs, L., Woychik, R.P.

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A New Mouse Insertional Mutation That Causes Sensorineural Deafness and Vestibular Defects von Alagramam, K. N, Kwon, H. Y, Cacheiro, N. L. A, Stubbs, L, Wright, C. G, Erway, L. C, Woychik, R. P

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Clarin‐2 is essential for hearing by maintaining stereocilia integrity and function von Dunbar, L.A, Patni, P, Aguilar, C, Mburu, P, Corns, L, Wells, H.R.R, Delmaghani, S, Parker, A, Johnson, S, Williams, D, Esapa, C.T, Simon, M.M, Chessum, L, Newton, S, Dorning, J, Jeyarajan, P, Morse, S, Lelli, A, Codner, G.F, Peineau, T, Gopal, S.R, Alagramam, K.N, Hertzano, R, Dulon, D, Wells, S, Williams, F.M, Petit, C, Dawson, S.J, Brown, S.D.M, Marcotti, W, El‐Amraoui, A, Bowl, M.R

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Mutations in Protocadherin 15 and Cadherin 23 Affect Tip Links and Mechanotransduction in Mammalian Sensory Hair Cells von Alagramam, K.N, Goodyear, R.J, Geng, R.S, Furness, D.N, van Aken, A.F.J, Marcotti, W, Kros, C.J, Richardson, G.P

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