A novel <it>WFS1 </it>mutation in a family with dominant low frequency sensorineural hearing loss with normal VEMP and EcochG findings
<p>Abstract</p> <p>Background</p> <p>Low frequency sensorineural hearing loss (LFSNHL) is an uncommon clinical finding. Mutations within three different identified genes (<it>DIAPH1, MYO7A</it>, and <it>WFS1</it>) are known to cause LFSNHL. The m...
| Main Authors: | , , , |
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| Format: | Article |
| Language: | English |
| Published: |
BMC
2008-06-01
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| Series: | BMC Medical Genetics |
| Online Access: | http://www.biomedcentral.com/1471-2350/9/48 |