- Article
GJB2 and GJB6 Genetic Variant Curation in an Argentinean Non-Syndromic Hearing-Impaired Cohort
- Paula Buonfiglio,
- Carlos D. Bruque,
- Leonela Luce,
- Florencia Giliberto,
- Vanesa Lotersztein,
- Sebastián Menazzi,
- Bibiana Paoli,
- Ana Belén Elgoyhen and
- Viviana Dalamón
Genetic variants in GJB2 and GJB6 genes are the most frequent causes of hereditary hearing loss among several deaf populations worldwide. Molecular diagnosis enables proper genetic counseling and medical prognosis to patients. In this study, we prese...

