Associated Papers
Ramifications of POU4F3 variants associated with autosomal dominant hearing loss in various molecular aspects.
Lee SY et al.
Scientific Reports, 2023
Genetic Load of Alternations of Transcription Factor Genes in Non-Syndromic Deafness and the Associated Clinical Phenotypes: Experience from Two Tertiary Referral Centers.
Jo HD et al.
Biomedicines, 2022
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