Genetics of Hearing Loss: Contributions of Mitochondrial DNA

No AccessPerspectives on Aural Rehabilitation and Its InstrumentationArticle1 Apr 2002Genetics of Hearing Loss: Contributions of Mitochondrial DNA Jill L. Elfenbein Jill L. Elfenbein Google Scholar More articles by this author https://doi.org/10.1044/arii10.1.2 SectionsAboutFull TextPDF ToolsAdd to favoritesDownload CitationTrack Citations ShareFacebookTwitterLinked In References Ballinger, S. W., Shoffner, J. M., Hedaya, E. V., Trounce, I., Polak, M. A., Koontz, D. A., & Wallace, D. C. (1992). Maternally transmitted diabetes and deafness associated with a 10.4 kb mitochondrial DNA deletion.Nature Genetics, 1, 11–15. Google Scholar Chinnery, P. F., Elliott, C., Green, G. R., Rees, A., Coulthard, A., Turnbull, D. M., & Griffiths, T. D. (2000). The spectrum of hearing loss due to mitochondrial DNA defects.Brain, 123, 82–92. Google Scholar Dirckx J. H. (2001). Stedman's concise medical dictionary for the health professions (4th ed.). Philadelphia: Lippincott Williams & Wilkins. 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