Analyses of GJB2 status in hereditary and non-syndromic hearing loss cases in Turkey reveal pathogenicity of rare c.247_249delTTC variant


Tümer S., ŞERBETÇİOĞLU M. B., KIRKIM G., Homurlu S. N., ALTUNGÖZ O.

International Journal of Pediatric Otorhinolaryngology, cilt.202, 2026 (SCI-Expanded, Scopus) identifier identifier