Literature DB >> 5157378

Familial low frequency hearing loss.

B W Konigsmark, M Mengel, C I Berlin.   

Abstract

Entities:  

Mesh：

Year:  1971        PMID： 5157378     DOI： 10.1288/00005537-197105000-00017

Source DB:  PubMed          Journal:  Laryngoscope        ISSN： 0023-852X            Impact factor:   3.325


× No keyword cloud information.
  4 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

4.  Tinnitus and 3-Year Change in Audiometric Hearing Thresholds.

Authors:  Sharon G Curhan; Christopher Halpin; Molin Wang; Roland D Eavey; Gary C Curhan
Journal:  Ear Hear       Date:  2021 July/Aug       Impact factor: 3.562
  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.