Varaico: Literature-Extracted Genetic Variants

Gene:POU3F4
Variant:p.W67*
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POU3F4

NM_000307.5:p.W67*

Associated Papers

Genotype and Outcomes of Cochlear Implantation in Children With Incomplete Partition Type III.

Chao X et al.

The Laryngoscope, 2025

Genomic and phenotypic landscapes of X-linked hereditary hearing loss in the Chinese population.

Feng H et al.

Orphanet Journal of Rare Diseases, 2024

A POU3F4 Mutation Causes Nonsyndromic Hearing Loss in a Chinese X-linked Recessive Family.

Du W et al.

Chinese Medical Journal, 2017

A novel mutation in POU3F4 in a Chinese family with X-linked non-syndromic hearing loss.

Huang BQ et al.

Journal of Otology, 2015

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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."