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Pengcheng Xu

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Open access Aug 2026

Two Novel Compound Heterozygous CDH23 Mutations Underlying Non-Syndromic Hearing Loss

Two novel compound heterozygous CDH23 mutations are identified in a thirteen-month-old girl with NSHL, expanding the known spectrum of CDH23 mutation and adding to the understanding of the genotype–phenotype correlations in NSHL.

Pengcheng Xu, Qi Liao, Yun Lin et al. · 0 citations

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