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注意：仅列出部分参考文献，下载原文获取全部文献信息。Hearing Loss Associated With Enlarged Vestibular Aqueduct and Zero or One Mutant Allele of SLC26A4
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Audiologic presentation of enlargement of the vestibular aqueduct according to the SLC26A4 genotypes
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Mouse Models for Pendrin-Associated Loss of Cochlear and Vestibular Function
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Extremely discrepant mutation spectrum of SLC26A4 between Chinese patients with isolated Mondini deformity and enlarged vestibular aqueduct
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Screening of SLC26A4, FOXI1 and KCNJ10 genes in unilateral hearing impairment with ipsilateral enlarged vestibular aqueduct
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Clinical characteristics and genotype-phenotype correlation of hearing loss patients with SLC26A4 mutations
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SLC26A4 gene is frequently involved in nonsyndromic hearing impairment with enlarged vestibular aqueduct in Caucasian populations
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SLC26A4/PDS genotype-phenotype correlation in hearing loss with enlargement of the vestibular aqueduct (EVA):: evidence that Pendred syndrome and non-syndromic EVA are distinct clinical and genetic entities
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