In silico and in vivo analyses of a novel variant in MYO6 identified in a family with postlingual non-syndromic hearing loss from Argentina.

NAR Genom Bioinform · 2024 · PMC11632615 · PMID 39664812

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highly significantP < 0.0001actually significant

This study revealed a highly significant difference with a P < 0.0001 when comparing MO-CON with MO, MO-WT-mRNA and MO-R925S-mRNA.

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Quoted from the open-access full text in Europe PMC under the licence the publisher applied. The sentence is reproduced exactly as published; the emphasis is ours.

<i>In silico</i> and <i>in vivo</i> analyses of a novel variant in <i>MYO</i>6 identified in a family with postlingual non-syndromic hearing loss from Argentina.

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