Hereditary cochleovestibular dysfunction due to a COCH gene mutation (DFNA9): a follow-up study of a family
Author:
Publisher
Wiley
Subject
Otorhinolaryngology
Reference29 articles.
1. 1 G. Van Camp, and R.J.H. Smith (2001 ) Hereditary Hearing Loss Home Homepage (HHH). URL. dnalab-http://www.uia.ac.be/dnalab/hhh
2. Non-Syndromal Autosomal Dominant Hearing Impairment: Ongoing Phenotypical Characterization of Genotypes
3. Autosomal Dominant Sensorineural Hearing Loss: Pedigrees, Audiologic Findings, and Temporal Bone Findings in Two Kindreds
4. Autosomal Dominant Sensorineural Hearing Loss: Further Temporal Bone Findings
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1. Interaural and sex differences in the natural evolution of hearing levels in pre-symptomatic and symptomatic carriers of the p.Pro51Ser variant in the COCH gene;Scientific Reports;2024-01-02
2. Efficient Delivery of Adeno-Associated Virus into Inner Ear In Vivo Through Trans-Stapes Route in Adult Guinea Pig;Human Gene Therapy;2022-07-01
3. Genotype-Phenotype Correlations of Pathogenic COCH Variants in DFNA9: A HuGE Systematic Review and Audiometric Meta-Analysis;Biomolecules;2022-01-27
4. A Novel COCH Mutation Affects the vWFA2 Domain and Leads to a Relatively Mild DFNA9 Phenotype;Otology & Neurotology;2020-12-29
5. A systematic review of hearing and vestibular function in carriers of the Pro51Ser mutation in the COCH gene;European Archives of Oto-Rhino-Laryngology;2019-02-26
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