An exceptional cause for the coexistence of chronic kidney disease with progressive sensorineural hearing loss: double mutations in the PKD2 and GJB2 genes

Kaynar R. K., Ertan H., Dibe E., Çıkrıkçı Ö.

The Egyptian Journal of Internal Medicine, vol.37, pp.167-171, 2025 (ESCI)

• Publication Type: Article / Case Report
• Volume: 37
• Publication Date: 2025
• Journal Name: The Egyptian Journal of Internal Medicine
• Journal Indexes: Emerging Sources Citation Index (ESCI)
• Page Numbers: pp.167-171
• Open Archive Collection: AVESIS Open Access Collection
• Karadeniz Technical University Affiliated: Yes