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A novel mutation in the WFS1 gene identified in a large Chinese family with low-frequency hearing im
[会议论文] 作者：Ti-zhen Yan,Ning Tang,Xiang-rong Tang,Wu-gao Li,Zhe-tao Li,Shi-qiang Luo,Yan Yang,Jmg-wen Li,Ji-wei Huang,
来源：第十四次全国医学遗传学学术会议 年份：2015
Background: Wolfram syndrome gene 1 (WFS1) accounts for most of the familial nonsyndromic low-frequency sensorineural hearing loss (LFSNHL) which is characterized by sensorineural hearing losses equal...
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