The molecular genetics of inherited deafness – current and future applications-Reference-Cited by-同舟云学术

The molecular genetics of inherited deafness – current and future applications

Published:1998-06 Issue:6 Volume:112 Page:523-530
ISSN:0022-2151
Container-title:The Journal of Laryngology & Otology
language:en
Short-container-title:J. Laryngol. Otol.

Author:

Bussoli Tracy J.,Steel Karen P.

Publisher

Cambridge University Press (CUP)

Subject

Otorhinolaryngology,General Medicine

Reference72 articles.

1. Pendred syndrome is caused by mutations in a putative sulphate transporter gene (PDS)

2. Prelingual Deafness: High Prevalence of a 30delG Mutation in the Connexin 26 Gene

3. Schacht J. (1998) Mechanism and prevention of aminoglyco-side-induced hearing loss. Association for Research in Otolaryngology. St Petersburg Beach Florida. Meeting Abstract No.2.

4. Association Between X-Linked Mixed Deafness and Mutations in the POU Domain Gene POU3F4

5. Mutation in Transcription Factor POU4F3 Associated with Inherited Progressive Hearing Loss in Humans

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5. Connexin 26 preverbal hearing impairment: Mutation prevalence and heterozygosity in a selected population: Problemas auditivos preverbales por Conexina 26: Prevalencia de mutacion y heterocigosidad en una población seleccionada;International Journal of Audiology;2002-01