Konu "Unilateral Progressive Hearing Loss" için Araştırma Çıktıları | TR-Dizin | WoS | Scopus | PubMed listeleme
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Unusual phenotype in 35delG mutation: a case report
(2024)Background: Mutations in the GJB2 gene, which encodes the protein connexin 26 and is involved in inner ear homeostasis, are identified in approximately 50% of patients with autosomal recessive nonsyndromic hearing loss, ...