Associated Papers
Novel OTOG Variants and Clinical Features of Hearing Loss in a Large Japanese Cohort.
Arai Y et al.
Genes, 2025
Identifying pathogenic variants in rare pediatric neurological diseases using exome sequencing.
Komatsu K et al.
Scientific Reports, 2024
39433808 (PubMed )
Supplement: 41598_2024_75020_MOESM2_ESM.xlsx › Supplementary_Table_S1
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