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NGS-based identification of a MYO7A mutation in a Korean family with DFNB2, a subtype of autosomal recessive non-syndromic hearing loss

Crossref DOI link: https://doi.org/10.1007/s13258-025-01653-8

Published Online: 2025-06-26

Published Print: 2025-08

Update policy: https://doi.org/10.1007/springer_crossmark_policy

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