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Rare Missense Variants in<i>MYO7A</i>and<i>OTOP2</i>Genes in a South Korean Meniere Disease Cohort

2025-06-17

Abstract excerpt

<h4>ABSTRACT</h4> Meniere disease (MD) is a polygenic condition defined by episodes of vertigo associated with sensorineural hearing loss and tinnitus. Genetic studies in familial MD in East Asian population are limited and the potential MD genes remain to be established in non-Finnish European populations. By exome sequencing and rare variant analysis, we search for existing and novel genes associated with MD in...

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Literature Corpus work: 275d673b-4b2b-59a0-9f56-436454224972
DOI: 10.1101/2025.06.16.25329383

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