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P459: Exome sequencing analysis reveals enrichment of variants in known autosomal dominant hearing loss genes in patients with presbycusis

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Bibliográfalaš dieđut
Váldodahkkit: Stefan Farrugia, Rory Olson, Eric Klee, Lisa Schimmenti
Materiálatiipa: Artigo
Giella:Inglês
Almmustuhtton: Elsevier 2023-01-01
Ráidu:Genetics in Medicine Open
Liŋkkat:http://www.sciencedirect.com/science/article/pii/S294977442300506X
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