Associated Papers
Different Contribution of Missense and Loss-of-Function Variants to the Genetic Structure of Familial and Sporadic Meniere Disease.
Parra-Perez AM et al.
Medcomm, 2025
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Supplement: MCO2-6-e70394-s001.xlsx › TableS13
Hypomorphic variants of cationic amino acid transporter 3 in males with autism spectrum disorders.
Nava C et al.
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Supplement: 726_2015_2057_MOESM2_ESM.xlsx › Sup_Table_3
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