A novel mutation in the <it>WFS1 </it>gene identified in a Taiwanese family with low-frequency hearing impairment

• मुख्य लेखकों: Chung Shing-Fang (लेखक), Wang Ying-Piao (लेखक), Tsai Hsun-Tien (लेखक), Lin Hung-Ching (लेखक), Ho Guan-Min (लेखक), Shu Min-Tsan (लेखक)
• स्वरूप: पुस्तक
• प्रकाशित: BMC, 2007-05-01T00:00:00Z.
• विषय: article
• ऑनलाइन पहुंच: Connect to this object online.

<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...