A <i>KCNQ4</i> c.546C>G Genetic Variant Associated with Late Onset Non-Syndromic Hearing Loss in a Taiwanese Population.

Genes (Basel) · 2021 · PMC8618107 · PMID 34828318

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did not reach statistical significanceno p-value reported

Although the risk did not reach statistical significance, we did observe SNHL in multiple unrelated patients with the c.546C>G variant.

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