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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Medcomm, 2025
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Supplement: MCO2-6-e70394-s001.xlsx › TableS13
Diverse monogenic subforms of human spermatogenic failure.
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Supplement: 41467_2022_35661_MOESM3_ESM.xlsx › Supplementary_Data_1
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