A novel dominant GJB2 (DFNA3) mutation in a Chinese family
Sign Up to like & getrecommendations! Published in 2017 at "Scientific Reports"
DOI: 10.1038/srep34425
Abstract: To decipher the phenotype and genotype of a Chinese family with autosomal dominant non-syndromic hearing loss (ADNSHL) and a novel dominant missense mutation in the GJB2 gene (DFNA3), mutation screening of GJB2 was performed on… read more here.
Keywords: chinese family; family; dfna3 mutation; novel dominant ... See more keywords