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Objective
KCNQ4 is one of the most common disease‐causing genes involved in autosomal dominant non‐syndromic hearing loss. We previously found that patients with KCNQ4 p.G285S exhibited a much more rapid deterioration in hearing loss than those with other KCNQ4 variants. To determine the rate of hearing loss and assess the disease for further analysis, we performed a long‐term follow‐up of these...