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ArticleMolecular genetics & genomic medicine2024

A novel variant c.902C>A (p. A301D) in KCNQ4 associated with non-syndromic deafness 2A in a Chinese family.

Lingyan Ren et al.PubMed ↗Full text ↗Publisher ↗

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2024
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Full record →Abstract, authors, funding and every citing paper · PMID 38980994