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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Detalles Bibliográficos
Autores principales: Tsai, Hsun-Tien, Wang, Ying-Piao, Chung, Shing-Fang, Lin, Hung-Ching, Ho, Guan-Min, Shu, Min-Tsan
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2007
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1890544/
https://www.ncbi.nlm.nih.gov/pubmed/17517145
http://dx.doi.org/10.1186/1471-2350-8-26

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1890544/
https://www.ncbi.nlm.nih.gov/pubmed/17517145
http://dx.doi.org/10.1186/1471-2350-8-26

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