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

Autor: Verrall Aimee M, Kallman Jeremy C, Bramhall Naomi F, Street Valerie A

Publikováno v: BMC Medical Genetics, Vol 9, Iss 1, p 48 (2008)

Abstract Background Low frequency sensorineural hearing loss (LFSNHL) is an uncommon clinical finding. Mutations within three different identified genes (DIAPH1, MYO7A, and WFS1) are known to cause LFSNHL. The majority of hereditary LFSNHL is associa

Externí odkaz: https://doaj.org/article/c5902a28b193473a9eabe1db34ae0bc9

Vestibular function in families with inherited autosomal dominant hearing loss.

Autor: Street, Valerie A.¹ vastreet@u.washington.edu, Kallman, Jeremy C.¹, Strombom, Paul D.², Bramhall, Naomi F.³, Phillips, James O.¹

Publikováno v: Journal of Vestibular Research: Equilibrium & Orientation. 2008, Vol. 18 Issue 1, p51-58. 8p. 2 Charts, 2 Graphs.

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In Search of the DFNA11Myosin VIIA Low- and Mid-Frequency Auditory Genetic Modifier

Autor: Kallman, Jeremy C., Phillips, James O., Bramhall, Naomi F., Kelly, John P., Street, Valerie A.

Publikováno v: Otology & Neurotology; September 2008, Vol. 29 Issue: 6 p860-867, 8p

Vestibular function in families with inherited autosomal dominant hearing loss.

Autor: Street VA; V.M. Bloedel Hearing Research Center, Otolaryngology - HNS Department, University of Washington, Seattle, WA 98195-5060, USA. vastreet@u.washington.edu, Kallman JC, Strombom PD, Bramhall NF, Phillips JO

Publikováno v: Journal of vestibular research : equilibrium & orientation [J Vestib Res] 2008; Vol. 18 (1), pp. 51-8.