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Open Access Research article

A novel WFS1 mutation in a family with dominant low frequency sensorineural hearing loss with normal VEMP and EcochG findings

Naomi F Bramhall, Jeremy C Kallman, Aimee M Verrall and Valerie A Street*

BMC Medical Genetics 2008, 9:48  doi:10.1186/1471-2350-9-48

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