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...
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| Main Authors: | , , , |
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| Format: | Book |
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BMC,
2008-06-01T00:00:00Z.
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Connect to this object online.3rd Floor Main Library
| Call Number: |
A1234.567 |
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| Copy 1 | Available |