Identification of a novel mutation in the SLC26A4 gene in an Italian with fluctuating sensorineural hearing loss-Reference-Cited by-同舟云学术

Identification of a novel mutation in the SLC26A4 gene in an Italian with fluctuating sensorineural hearing loss

Published:2009-10 Issue:10 Volume:73 Page:1458-1463
ISSN:0165-5876
Container-title:International Journal of Pediatric Otorhinolaryngology
language:en
Short-container-title:International Journal of Pediatric Otorhinolaryngology

Author:

Cama Elona,Alemanno Maria Stella,Bellacchio Emanuele,Santarelli Rosamaria,Carella Massimo,Zelante Leopoldo,Palladino Teresa,Inches Ingrid,di Paola Francesco,Arslan Edoardo,Melchionda Salvatore

Publisher

Elsevier BV

Subject

Otorhinolaryngology,General Medicine,Pediatrics, Perinatology, and Child Health

Reference41 articles.

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4. Pendred syndrome is caused by mutations in a putative sulphate transporter gene (PDS);Everett;Nat. Genet.,1997

5. The solute carrier 26 family of proteins in epithelial ion transport;Dorwart;Physiology,2008

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1. Mapping pathogenic mutations suggests an innovative structural model for the pendrin (SLC26A4) transmembrane domain;Biochimie;2017-01

2. Identification of a novel mutation in SLC26A4 gene in a Chinese family with enlarged vestibular aqueduct syndrome;International Journal of Pediatric Otorhinolaryngology;2016-06

3. Sordità fluttuanti;EMC - Otorinolaringoiatria;2014-06

4. Hipoacusias fluctuantes;EMC - Otorrinolaringología;2014-04

5. Molecular analysis of SLC26A4 gene in patients with nonsyndromic hearing loss and EVA: Identification of two novel mutations in Brazilian patients;International Journal of Pediatric Otorhinolaryngology;2013-03