Varaico: Literature-Extracted Genetic Variants

Gene:CLDN9
Variant:p.C25W
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CLDN9

NM_020982.4:p.C25W

Associated Papers

Variants of human CLDN9 cause mild to profound hearing loss.

Ramzan M et al.

Human Mutation, 2021

Identification of Novel Candidate Genes and Variants for Hearing Loss and Temporal Bone Anomalies.

Santos-Cortez RLP et al.

Genes, 2021

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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."