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.· Audiology Research· 0 citations
How degraded acoustic input shifts processing from rapid, implicit lexical access toward explicit working-memory-dependent reconstruction within the Ease of Language Understanding (ELU) model is described.
D. Monzani, Andrea Bianchino, A. Ciorba et al.· Journal of Intelligence· 0 citations
A review of the English literature to date on hearing loss and Pendred syndrome offers clinicians a practical tool for a feasible and early diagnosis, offering clinicians a practical tool for a feasible and early diagnosis.
Marianna Manuelli, Andrea Migliorelli, C. Bianchini et al.· The journal of international...· 0 citations
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