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A novel mutation in the WFS1 gene identified in a Taiwanese family with low-frequency hearing impairment
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 b...
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| Main Authors: | , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2007
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1890544/ https://ncbi.nlm.nih.gov/pubmed/17517145 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2350-8-26 |
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