Author

Yun Lin

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Open access Aug 2026

Clinical and Genetic Features in EYA1-Associated Branchio-Oto Syndrome: Cochlear Nerve Deficiency in Five of Thirteen Patients

It is suggested that CND may be a relatively common radiologic feature in EYA1-associated BOS, particularly among patients with truncating variants or large deletions, although larger studies are needed to confirm this association.

Yi-Rong Niu, Yun Lin, Jiali Yu et al. · Diagnostics · 0 citations

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. · International Journal of Gen... · 0 citations