Fluctuating sensorineural hearing loss associated with enlarged vestibular aqueduct maps to 7q31, the region containing the pendred gene
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference37 articles.
1. Three Familial Cases of Hearing Loss Associated with Enlargement of the Vestibular Aqueduct
2. Linkage of congenital, recessive deafness (DFNB4) to chromosome 7q31 and evidence for genetic heterogeneity in the Middle Eastern Druze population
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1. Non-syndromic enlarged vestibular aqueduct caused by novel compound mutations of the SLC26A4 gene: a case report and literature review;Frontiers in Genetics;2023-09-07
2. A whole-exome analysis of non-syndromic hearing loss patients from India reveals a wide spectrum of known and novel mutations;2023-02-10
3. Analysis of SLC26A4, FOXI1, and KCNJ10 Gene Variants in Patients with Incomplete Partition of the Cochlea and Enlarged Vestibular Aqueduct (EVA) Anomalies;International Journal of Molecular Sciences;2022-12-06
4. The incidence of enlarged vestibular aqueduct among hearing-impaired children: hospital-based tertiary care referral center;The Egyptian Journal of Otolaryngology;2022-10-29
5. Contralateral hearing loss in children with a unilateral enlarged vestibular aqueduct;International Journal of Pediatric Otorhinolaryngology;2021-11
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