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 5 publications that cite this research output on Dimensions.
Reevaluating the splice-altering variant in TECTA as a cause of nonsyndromic hearing loss DFNA8/12 by functional analysis of RNA
Preprint in Research Square (November 2023)
Preimplantation Genetic Testing (PGT) and Prenatal Diagnosis of Schaaf-Yang Syndrome: A Report of Three Families and a Research on Genotype–Phenotype Correlations
Article in Journal of Clinical Medicine (February 2023)