【摘 要】
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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
【机 构】
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Key Laboratory of birth defects prevention and control, Liuzhou, Guangxi 545001, P.R.China;Departmen
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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 to and below 2000 Hz.The current study aimed to contribute to our understanding of the molecular basis of LFSNHL in an affected Chinese family.
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