A novel WFS1 mutation in a family with dominant low frequency sensorineural hearing loss with normal VEMP and EcochG findings.
| Autor: | Bramhall, Naomi F.1 nbramh@u.washington.edu, Kallman, Jeremy C.2 jeremyk@u.washington.edu, Verrall, Aimee M.2 verrall@u.washington.edu, Street, Valerie A.2 vastreet@u.washington.edu |
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| Zdroj: | BMC Medical Genetics. 2008, Vol. 9, Special section p1-6. 6p. 1 Graph. |
| Databáze: | Academic Search Ultimate |
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