Low Frequency Hearing Loss and Genetic Modifiers in an American Family

No AccessPerspectives on AudiologyArticle1 May 2005Low Frequency Hearing Loss and Genetic Modifiers in an American Family Valerie Street Valerie Street Bloedel Hearing Research Center, University of Washington, Seattle Google Scholar More articles by this author https://doi.org/10.1044/poa1.1.14 SectionsAboutFull TextPDF ToolsAdd to favoritesDownload CitationTrack Citations ShareFacebookTwitterLinked In References Bespalova, I. N., Van Camp, G.,Bom, S. J.,Brown, D. J.,Cryns, K., DeWan, A. T.,Erson, A. E.,Flothmann, K.,Kunst, H. P.,Kurnool, P.,Sivakumaran, T. A.,Cremers, C. W.,Leal, S. M.,Burmeister, M., & Lesperance, M. M. (2001). Mutations in the Wolfram syndrome 1 gene (WFS1) are a common cause of low frequency sensorineural hearing loss..Human Molecular Genetics,, 10,2501–2508. Google Scholar Bolz, H.,Bolz, S. S.,Schade, G.,Kothe, C.,Mohrmann, G.,Hess, M., & Gal, A. (2004). 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Non-syndromic progressive hearing loss DNFA38 is caused by heterozygous missense mutation in the Wolfram syndrome gene WFS1..Human Molecular Genetics,( 10(22), 2509–2514. Google Scholar Additional Resources FiguresReferencesRelatedDetails Volume 1Issue 1May 2005Pages: 14-18 Get Permissions Add to your Mendeley library History Published in issue: May 1, 2005 Metrics Topicsasha-topicsasha-article-typesleader-topicsCopyright & PermissionsCopyright © 2005 American Speech-Language-Hearing AssociationPDF downloadLoading ...