Autosomal Dominant Low-Frequency Hearing Impairment (DFNA6/14)-Reference-Cited by-同舟云学术

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Autosomal Dominant Low-Frequency Hearing Impairment (DFNA6/14)

Published:2002-11 Issue:6 Volume:23 Page:876-884
ISSN:1531-7129
Container-title:Otology & Neurotology
language:en
Short-container-title:Otology & Neurotology

Author:

Bom Steven J. H.,Van Camp Guy,Cryns Kim,Admiraal Ronald J. C.,Huygen Patrick L. M.,Cremers Cor W. R. J.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Neurology (clinical),Sensory Systems,Otorhinolaryngology

Reference14 articles.

1. Genetic Epidemiology of Hearing Impairment

2. Non-Syndromal Autosomal Dominant Hearing Impairment: Ongoing Phenotypical Characterization of Genotypes

3. The gene for an inherited form of deafness maps to chromosome 5q31.

4. A gene for autosomal dominant nonsyndromic hereditary hearing impairment maps to 4p16.3

Cited by 15 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. Genotype and Phenotype Analyses of a Novel WFS1 Variant (c.2512C>T p.(Pro838Ser)) Associated with DFNA6/14/38;Genes;2023-02-10

2. Whole exome sequencing identifies a pathogenic mutation in WFS1 in two large Chinese families with autosomal dominant all-frequency hearing loss and prenatal counseling;International Journal of Pediatric Otorhinolaryngology;2018-03

3. Audioprofile Surfaces;Annals of Otology, Rhinology & Laryngology;2015-11-03

4. WFS1 mutations in hearing-impaired children;International Journal of Audiology;2014-03-10

5. Comorbidity of GJB2 and WFS1 mutations in one family;Gene;2012-06

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