Vertical Corneal Striae in Families with Autosomal Dominant Hearing Loss: DFNA9/COCH
Author:
Publisher
Elsevier BV
Subject
Ophthalmology
Reference40 articles.
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4. A new autosomal dominant syndrome of idiopathic progressive vestibulo-cochlear dysfunction with middle-age onset;Verhagen;Acta Otolaryngol,1992
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1. Genotype-Phenotype Correlations of Pathogenic COCH Variants in DFNA9: A HuGE Systematic Review and Audiometric Meta-Analysis;Biomolecules;2022-01-27
2. 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
3. Does Otovestibular Loss in the Autosomal Dominant Disorder DFNA9 Have an Impact of on Cognition? A Systematic Review;Frontiers in Neuroscience;2018-01-09
4. Molecular Description of Eye Defects in the Zebrafish Pax6b Mutant, sunrise, Reveals a Pax6b-Dependent Genetic Network in the Developing Anterior Chamber;PLOS ONE;2015-02-18
5. A novel COCH mutation associated with autosomal dominant nonsyndromic hearing loss disrupts the structural stability of the vWFA2 domain;Journal of Molecular Medicine;2012-05-19
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