Subgroups of enlarged vestibular aqueduct in relation toSLC26A4mutations and hearing loss-Reference-Cited by-同舟云学术

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Subgroups of enlarged vestibular aqueduct in relation toSLC26A4mutations and hearing loss

Published:2013-12-17 Issue:4 Volume:124 Page:E134-E140
ISSN:0023-852X
Container-title:The Laryngoscope
language:en
Short-container-title:The Laryngoscope

Author:

Okamoto Yasuhide¹²³,Mutai Hideki¹,Nakano Atsuko⁴,Arimoto Yukiko⁴,Sugiuchi Tomoko⁵,Masuda Sawako⁶,Morimoto Noriko⁷,Sakamoto Hirokazu⁸,Ogahara Noboru⁹,Takagi Akira¹⁰,Taiji Hidenobu⁷,Kaga Kimitaka¹,Ogawa Kaoru³,Matsunaga Tatsuo¹

Affiliation:

1. Department of Otolaryngology; National Hospital Organization Tokyo Medical Center; Tokyo Japan

2. Department of Otorhinolaryngology; Inagi Municipal Hospital; Tokyo Japan

3. Department of Otolaryngology; Keio University Hospital; Tokyo Japan

4. Division of Otorhinolaryngology; Chiba Children's Hospital; Chiba Japan

5. Department of Otolaryngology; Kanto Rosai Hospital; Kanagawa Japan

6. Department of Otorhinolaryngology; National Mie Hospital; Mie Japan

7. Department of Otorhinolaryngology; National Center for Children and Development; Tokyo Japan

8. Department of Otorhinolaryngology; Kobe Children's Hospital; Hyogo Japan

9. Department of Otorhinolaryngology; Kanagawa Children's Medical Center; Kanagawa Japan

10. Department of Otorhinolaryngology; Shizuoka General Hospital Shizuoka Japan

Publisher

Wiley

Subject

Otorhinolaryngology

Reference26 articles.

1. Enlarged vestibular aqueduct syndrome in the pediatric population;Madden;Otol Neurotol,2003

2. The influence of mutations in the SLC26A4 gene on the temporal bone in a population with enlarged vestibular aqueduct;Madden;Arch Otolaryngol Head Neck Surg,2007

3. SLC26A4/PDS genotype-phenotype correlation in hearing loss with enlarged vestibular aqueduct (EVA): evidence that Pendred syndrome and non-syndromic EVA are distinct clinical and genetic entities;Pryor;J Med Genet,2005

4. Genotype-phenotype correlations for SLC26A4-related deafness;Azaiez;Hum Genet,2007

5. Hypo-functional SLC26A4 variants associated with nonsyndromic hearing loss and enlarged vestibular aqueduct: genotype-phenotype correlation or coincidental polymorphisms?;Choi;Hum Mutat,2009

Cited by 25 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. Classifying the Large Vestibular Aqueduct: Morphometry to Audiometry;Otology & Neurotology;2023-01

2. Selection of Diagnostically Significant Regions of the SLC26A4 Gene Involved in Hearing Loss;International Journal of Molecular Sciences;2022-11-03

3. Clinical and genetic analysis of children with hearing loss and bilateral enlarged vestibular aqueducts;International Journal of Pediatric Otorhinolaryngology;2022-01

4. Connexin 26 (GJB2) gene mutations linked with autosomal recessive non-syndromic sensor neural hearing loss in the Iraqi population;Journal of Medicine and Life;2021-12

5. Insights into phenotypic differences between humans and mice with p.T721M and other C-terminal variants of the SLC26A4 gene;Scientific Reports;2021-10-25

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