Radiologic Features in Cochlear Implant Candidates: A Prospective Study Comparing Candidates Carrying the p.Pro51Ser Mutation in Coagulation Factor C Homology With Noncarriers
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Neurology (clinical),Sensory Systems,Otorhinolaryngology
Reference29 articles.
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2. Potential treatments for genetic hearing loss in humans: current conundrums;Gene Ther,2015
3. Genotype-phenotype correlation study in a large series of patients carrying the p.Pro51Ser (p.P51S) variant in COCH (DFNA9) part II: a prospective cross-sectional study of the vestibular phenotype in 111 carriers;Ear Hear,2021
4. Genotype-phenotype correlation study in a large series of patients carrying the p.Pro51Ser (p.P51S) variant in COCH (DFNA9): part I—a cross-sectional study of hearing function in 111 carriers;Ear Hear,2021
5. A systematic review of hearing and vestibular function in carriers of the Pro51Ser mutation in the COCH gene;Eur Arch Otorhinolaryngol,2019
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