Role of Protein Misfolding in DFNA9 Hearing Loss
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry
Reference31 articles.
1. Molecular pathways to neurodegeneration
2. Mutations in a novel cochlear gene cause DFNA9, a human nonsyndromic deafness with vestibular dysfunction
3. Histopathology of the Inner Ear in DFNA9
4. Autosomal Dominant Sensorineural Hearing Loss: Pedigrees, Audiologic Findings, and Temporal Bone Findings in Two Kindreds
5. Mapping and Characterization of a Novel Cochlear Gene in Human and in Mouse: A Positional Candidate Gene for a Deafness Disorder, DFNA9
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1. Rational design of a genomically humanized mouse model for dominantly inherited hearing loss, DFNA9;Hearing Research;2024-02
2. 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
3. A Novel COCH p.D544Vfs*3 Variant Associated with DFNA9 Sensorineural Hearing Loss Causes Pathological Multimeric Cochlin Formation;Life;2023-12-25
4. Construction of mouse cochlin mutants with different GAG-binding specificities and their use for immunohistochemistry;Biochemical Journal;2023-01-06
5. Radiologic Features in Cochlear Implant Candidates: A Prospective Study Comparing Candidates Carrying the p.Pro51Ser Mutation in Coagulation Factor C Homology With Noncarriers;Otology & Neurotology;2022-08-20
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