A novel mutation in the <it>WFS1 </it>gene identified in a Taiwanese family with low-frequency hearing impairment
<p>Abstract</p> <p>Background</p> <p>Wolfram syndrome gene 1 (<it>WFS1</it>) accounts for most of the familial nonsyndromic low-frequency sensorineural hearing loss (LFSNHL) which is characterized by sensorineural hearing losses equal to and below 2000 Hz. T...
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| Main Authors: | , , , , , |
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| Format: | Book |
| Published: |
BMC,
2007-05-01T00:00:00Z.
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| Online Access: | Connect to this object online. |
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