The Role of Pendrin in the Development of the Murine Inner Ear
Author:
Publisher
S. Karger AG
Subject
Physiology
Reference48 articles.
1. The Large Vestibular Aqueduct Syndrome
2. Comprehensive molecular etiology analysis of nonsyndromic hearing impairment from typical areas in China
3. Phenotypic Analyses and Mutation Screening of the SLC26A4 and FOXI1 Genes in 101 Taiwanese Families with Bilateral Nonsyndromic Enlarged Vestibular Aqueduct (DFNB4) or Pendred Syndrome
4. Hypo-FunctionalSLC26A4variants associated with nonsyndromic hearing loss and enlargement of the vestibular aqueduct: Genotype-phenotype correlation or coincidental polymorphisms?
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1. Novel small molecule-mediated restoration of the surface expression and anion exchange activity of mutated pendrin causing Pendred syndrome and DFNB4;Biomedicine & Pharmacotherapy;2023-11
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4. Exploring the missing heritability in subjects with hearing loss, enlarged vestibular aqueducts, and a single or no pathogenic SLC26A4 variant;Human Genetics;2021-08-19
5. Interpreting pendred syndrome as a foetal hydrops: Clinical and animal model evidence;Journal of Vestibular Research;2021-07-28
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