Literature DB >> 5663381

Dominantly inherited low-frequency hearing loss.

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Year:  1968        PMID： 5663381

Source DB:  PubMed          Journal:  Arch Otolaryngol        ISSN： 0003-9977


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  5 in total

1.  Mutations in the Wolfram syndrome 1 gene (WFS1) are a common cause of low frequency sensorineural hearing loss.

Authors:  I N Bespalova; G Van Camp; S J Bom; D J Brown; K Cryns; A T DeWan; A E Erson; K Flothmann; H P Kunst; P Kurnool; T A Sivakumaran; C W Cremers; S M Leal; M Burmeister; M M Lesperance
Journal:  Hum Mol Genet       Date:  2001-10-15       Impact factor: 6.150

2.  Mutations in the Wolfram syndrome type 1 gene (WFS1) define a clinical entity of dominant low-frequency sensorineural hearing loss.

Authors:  Marci M Lesperance; James W Hall; Theresa B San Agustin; Suzanne M Leal
Journal:  Arch Otolaryngol Head Neck Surg       Date:  2003-04

Review 3.  Vestibular function in families with inherited autosomal dominant hearing loss.

Authors:  Valerie A Street; Jeremy C Kallman; Paul D Strombom; Naomi F Bramhall; James O Phillips
Journal:  J Vestib Res       Date:  2008       Impact factor: 2.435

4.  Autosomal dominant optic neuropathy and sensorineual hearing loss associated with a novel mutation of WFS1.

Authors:  Barend F T Hogewind; Ronald J E Pennings; Frans A Hol; Henricus P M Kunst; Elisabeth H Hoefsloot; Johannes R M Cruysberg; Cor W R J Cremers
Journal:  Mol Vis       Date:  2010-01-12       Impact factor: 2.367

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

Authors:  Naomi F Bramhall; Jeremy C Kallman; Aimee M Verrall; Valerie A Street
Journal:  BMC Med Genet       Date:  2008-06-02       Impact factor: 2.103
  5 in total

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