Clinical aspects of an autosomal dominantly inherited hearing impairment linked to the DFNA60 locus on chromosome 2q23.1

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Clinical aspects of an autosomal dominantly inherited hearing impairment linked to the DFNA60 locus on chromosome 2q23.1–2q23.3

Published:2013-06 Issue: Volume:300 Page:10-17
ISSN:0378-5955
Container-title:Hearing Research
language:en
Short-container-title:Hearing Research

Author:

van Beelen E.,Schraders M.,Huygen P.L.M.,Oostrik J.,Plantinga R.F.,van Drunen W.,Collin R.W.J.,Kooper D.P.,Pennings R.J.E.,Cremers C.W.R.J.,Kremer H.,Kunst H.P.M.

Publisher

Elsevier BV

Subject

Sensory Systems

Reference16 articles.

1. Vestibular deterioration precedes hearing deterioration in the P51S COCH mutation (DFNA9): an analysis in 74 mutation carriers;Bischoff;Otol. Neurotol.,2005

2. Missense mutations in POU4F3 cause autosomal dominant hearing impairment DFNA15 and affect subcellular localization and DNA binding;Collin;Hum. Mutat.,2008

3. Longitudinal and cross-sectional phenotype analysis in a new, large Dutch DFNA2/KCNQ4 family;De Leenheer;Ann. Otol. Rhinol. Laryngol.,2002

4. easyLINKAGE-Plus – automated linkage analyses using large-scale SNP data;Hoffmann;Bioinformatics,2005

5. Mapping of the alpha-tectorin gene (TECTA) to mouse chromosome 9 and human chromosome 11: a candidate for human autosomal dominant nonsyndromic deafness;Hughes;Genomics,1998

Cited by 1 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Non-syndromic hearing loss gene identification: A brief history and glimpse into the future;Molecular and Cellular Probes;2015-10

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