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Frontiers | DFNB1 Non-syndromic Hearing Impairment: Diversity of Mutations and Associated Phenotypes
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IJMS | Free Full-Text | Analysis of SLC26A4, FOXI1, and KCNJ10 Gene Variants in Patients with Incomplete Partition of the Cochlea and Enlarged Vestibular Aqueduct (EVA) Anomalies
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Frontiers | DFNB1 Non-syndromic Hearing Impairment: Diversity of Mutations and Associated Phenotypes
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