2026-08-252026-08-25https://scholars.csmu.edu.tw/handle/123456789/16957Recently, we identified novel heterozygous missense mutation, p.L10R, p.P18S, p.V84I, p.V174M, p.E183k and p.A194T, in the GJB3 gene encoding CX31 from 513 unrelated Taiwanese patients with non-sy...(詳)遺傳性聽障一種常見的感音神經性疾病，在開發中國家大約60%由於基因突變所造成的。目前已知有59個基因的突變會導致聽障且每個基因的致病機制皆不盡相同。gap junction在聽力功能上扮演的角...(詳)基因突變聽障功能研究斑馬魚GJB3mutationhearing lossgap junctionzebrafishresearch project