Varaico: Literature-Extracted Genetic Variants

Gene:COCH
Variant:p.G88A
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COCH

NM_004086.3:p.G88A

Associated Papers

Genes linked to hearing and vestibular phenotypes in humans and mice: an interspecies systematic review.

Ayoub C et al.

Human Genomics, 2025

41430327 (PubMed )
Supplement: 40246_2025_891_MOESM1_ESM.xlsx › Supplementary_Table_S2.

Hearing and Vestibular Impairment Related to a Variant (c.263G>C) of the COCH Gene.

Alonso AV et al.

Otolaryngology--head and Neck Surgery : Official Journal of American Academy of Otolaryngology-head and Neck Surgery, 2025

Clinical Impact of Genetic Diagnosis of Sensorineural Hearing Loss in Adults.

Corriols-Noval P et al.

Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology, 2022

Audiovestibular Phenotypes and Advanced Magnetic Resonance Imaging Features of Cochlin Gene Mutation Carriers.

Conte G et al.

Audiology & Neuro-otology, 2019

Diagnostic yield of genetic testing in adults with sensorineural hearing loss.

Reda Del Barrio S et al.

Acta Otorrinolaringologica Espanola, 0

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Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."