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G. Vitetta

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Review Open access Sep 2026

Updates in TECTA Mutation Spectrum: A Scoping Review

Background/Objectives: The TECTA gene variant is one of the most common causes of nonsyndromic congenital hearing loss affecting the mid-frequency range. Situated on chromosome 11q22–q24, the TECTA gene encodes α-tectorin, a non-collagenous protein of the tectorial membrane. Pathogenetic variants of TECTA are relativel...

Marianna Manuelli, Andrea Migliorelli, S. Pelucchi et al. · 0 citations

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