Mutations in the Wolfram syndrome 1 gene (WFS1) are a common cause of low frequency sensorineural hearing loss

Non-syndromic low frequency sensorineural hearing loss (LFSNHL) affecting only 2000 Hz and below is an unusual type of hearing loss that worsens over time without progressing to profound deafness. This type of LFSNHL may be associated with mild tinnitus but is not associated with vertigo. We have pr...

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Bibliografiset tiedot
Julkaisussa:Hum Mol Genet
Päätekijät: Bespalova, Irina N., Van Camp, Guy, Bom, Steven J.H., Brown, David J., Cryns, Kim, DeWan, Andrew T., Erson, Ayse E., Flothmann, Kris, Kunst, Henricus P.M., Kurnool, Purnima, Sivakumaran, Theru A., Cremers, Cor W.R.J., Leal, Suzanne M., Burmeister, Margit, Lesperance, Marci M.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 2001
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Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC6198816/
https://ncbi.nlm.nih.gov/pubmed/11709537
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