Associated Papers
Different Contribution of Missense and Loss-of-Function Variants to the Genetic Structure of Familial and Sporadic Meniere Disease.
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Supplement: MCO2-6-e70394-s001.xlsx › TableS13
Rare variants in cardiomyopathy genes predispose to cardiac injury in severe COVID-19 patients of African or Hispanic ancestry.
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NCOA3 identified as a new candidate to explain autosomal dominant progressive hearing loss.
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Human Molecular Genetics, 2021
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Supplement: supplementary_material_figure_legends_and_supplementary_tables_ddaa240.doc
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