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- W2912170268 abstract "No AccessPerspectives on Hearing and Hearing Disorders in ChildhoodEditorial1 Jul 2001Hereditary Hearing Impairment in Children: An Explosion of New Knowledge Emerging From the Human Genome Project and Mouse Models James F. Battey James F. Battey National Institute on Deafness and Other Communication DisordersBethesda, MD Google Scholar More articles by this author https://doi.org/10.1044/hhdc11.2.2 SectionsAboutFull TextPDF ToolsAdd to favoritesDownload CitationTrack Citations ShareFacebookTwitterLinked In References Avraham, K. B., Hasson, T., Steel, K. P.,Kingsley, D. M., Russell, L. B.,Mooseker, M. S.,Copeland, N. G., & Jenkins, N. A. (1995). The mouse Snell’s waltzer deafness gene encodes an unconventional myosin required for structural integrity of inner ear hair cells..Nature Genetics, 11, 369–375. Google Scholar Cohn, E. S.,Kelley, P. M.,Fowler, T. W.,Gorga, M. P.,Lefkowitz, D. M.,Kuehn, H. J.,Schaefer, G. B.,Gobar, L. S.,Hahn, F. 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B.,Morton, C. C.,Blumenfeld, A.,Frydman, M.,Friedman, T. B.,King, M.-C., & Avraham, K. B. (1998). Mutation in the transcription factor POU4F3 associated with inherited progressive hearing loss in humans..Science, 279, 1950–1953. Google Scholar Van Laer, L.,Huizing, E. H.,Verstreken, M.,van Zuijen, D.,Wauters, J. G.,Bossuyt, P. J.,Van de Heyning, P.,McGuirt, W. T.,Smith, R. J. H.,Willems, P. J.,Legan, P. K.,Richardson, G. P., & Van Camp, G. (1998). Non-syndromic hearing impairment is associated with a mutation in DFNA5..Nature Genetics, 20, 194–197. Google Scholar Verhoeven, K.,Laer, L. V.,Kirschofer, K. , Legan, P. K.,Hughes, D. C.,Schatteman, I.,Verstreken, M.,Van Hauwe, P.,Coucke, P.,Chen, A.,Smith, R. J. H.,Somers, T.,Offeciers, F. E.,Van de Heyning, P.,Richardson, G. P.,Wachtler, F.,Kimberling, W. J., Willems, P. J.,Govaerts, P. J., & Van Camp, G. (1998). Mutations in the human alpha-tectorin gene cause autosomal dominant non-syndromic hearing impairment.Nature Genetics, 19, 60–62. Google Scholar Wang, A.,Liang, Y.,Fridell, R. A.,Probst, F. J.,Wilcox, E. R.,Touchman, J. W.,Morton, C. C.,Morell, R. J., Noben-Trauth, K.,Camper, S. A., & Friedman, T. B. (1998). Association of unconventional myosin MYO15 mutations with human nonsyndromic deafness DFNB3. Science. 280, 1447–1451. Google Scholar Weil, D.,Blanchard, S.,Kaplan, J.,Guilford, P.,Gibson, F.,Walsh, J.,Mburu, P.,Varela, A.,Levilliers, J.,Weston, M. D.,Kelley, P. M.,Kimberling, W. J.,Wagenar, M.,Levi-Acobas, F.,Larget-Piet, D.,Munnich, A.,Steel, K. P.,Brown, S. D. M., & Petit, C. (1995). Defective myosin VIIA gene responsible for Usher syndrome 1B..Nature, 274, 60–61. Google Scholar Weil, D.,Kussel, P.,Blanchard, S.,Levy, G.,Levi-Acobas, F.,Drira, M.,Ayadi, H., & Petit, C. (1997). The autosomal resessive isolated deafness, DFNB2, and the Usher 1B syndrome are allelic defects of the myosin-VIIA gene..Nature Genetics, 16, 191–193. Google Scholar Zheng, Q.-Y., Johnson, K., & Erway, L. (1999). Assessment of hearing in 80 inbred strains of mice by ABR threshold analyses..Hearing Research, 130, 94–107. Google Scholar Additional Resources FiguresReferencesRelatedDetails Volume 11Issue 2July 2001Pages: 2-7 Get Permissions Add to your Mendeley library History Published in issue: Jul 1, 2001 Metrics Topicsasha-topicsleader-topicsasha-article-typesasha-sigsCopyright & Permissions© 2001 American Speech-Language-Hearing AssociationPDF DownloadLoading ..." @default.
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