Reevaluating the splice-altering variant in TECTA as a cause of nonsyndromic hearing loss DFNA8/12 by functional analysis of RNA
Article in Human Molecular Genetics (April 2024)
The most recent citing publications are shown below. View all 45 publications that cite this research output on Dimensions.
Clinical relevance of the TECTA c.6183G>T variant identified in a family with autosomal dominant hearing loss: a case report
Article in Croatian Medical Journal (October 2023)
Autosomal Dominant Non-Syndromic Hearing Loss (DFNA): A Comprehensive Narrative Review
Article in Biomedicines (June 2023)