Literature DB >> 6026952

Sensorineural hearing loss for low tones.

T Iinuma, T Shitara, T Hoshino, I Kirikae.   

Abstract

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Year:  1967        PMID： 6026952     DOI： 10.1001/archotol.1967.00760050112023

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


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  3 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

3.  Low frequency hereditary deafness in man with childhood onset.

Authors:  P E León; J A Bonilla; J R Sánchez; R Vanegas; M Villalobos; L Torres; F León; A L Howell; J A Rodríguez
Journal:  Am J Hum Genet       Date:  1981-03       Impact factor: 11.025
  3 in total

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