Progressive Late-Onset Sensorineural Hearing Loss and Vestibular Impairment with Vertigo (DFNA9/COCH): Longitudinal Analyses in a Belgian Family-Reference-Cited by-同舟云学术

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Progressive Late-Onset Sensorineural Hearing Loss and Vestibular Impairment with Vertigo (DFNA9/COCH): Longitudinal Analyses in a Belgian Family

Published:2003-09 Issue:5 Volume:24 Page:743-748
ISSN:1531-7129
Container-title:Otology & Neurotology
language:en
Short-container-title:Otology & Neurotology

Author:

Lemaire Francois X.,Feenstra Louw,Huygen Patrick L. M.,Fransen Erik,Devriendt Koen,Van Camp Guy,Vantrappen Greet,Cremers Cor W. R. J.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Clinical Neurology,Sensory Systems,Otorhinolaryngology

Reference16 articles.

1. A gene for non-syndromic autosomal dominant progressive postlingual sensorineural hearing loss maps to chromosome 14q12-13

2. A New Autosomal Dominant Syndrome of Idiopathic Progressive Vestibulo-cochlear Dysfunction with Middle-age Onset

3. Familial Progressive Vestibulocochlear Dysfunction

4. Hereditary vestibulo-cochlear dysfunction and vascular disorders

5. A Pro51Ser mutation in the COCH gene is associated with late onset autosomal dominant progressive sensorineural hearing loss with vestibular defects

Cited by 30 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

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. Genotype-Phenotype Correlations of Pathogenic COCH Variants in DFNA9: A HuGE Systematic Review and Audiometric Meta-Analysis;Biomolecules;2022-01-27

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 & Hearing;2021-10-22

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 & Hearing;2021-10-22

5. Homozygote loss-of-function variants in the human COCH gene underlie hearing loss;European Journal of Human Genetics;2020-09-16

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