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

<p>Abstract</p> <p>Background</p> <p>Low frequency sensorineural hearing loss (LFSNHL) is an uncommon clinical finding. Mutations within three different identified genes (<it>DIAPH1, MYO7A</it>, and <it>WFS1</it>) are known to cause LFSNHL. The majority of hereditary LFSNHL is associated with hetero...

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Autori principali:	Verrall Aimee M, Kallman Jeremy C, Bramhall Naomi F, Street Valerie A
Natura:	Artigo
Lingua:	Inglês
Pubblicazione:	BMC 2008-06-01
Serie:	BMC Medical Genetics
Accesso online:	http://www.biomedcentral.com/1471-2350/9/48
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