Single nucleotide polymorphisms of the GJB2 and GJB6 genes are associated with autosomal recessive nonsyndromic hearing loss. [electronic resource]
- BioMed research international 2015
- 318727 p. digital
Publication Type: Clinical Trial; Journal Article; Research Support, Non-U.S. Gov't
2314-6141
10.1155/2015/318727 doi
Connexin 26 Connexin 30 Connexins--genetics Deafness--genetics Female Genetic Diseases, Inborn--genetics Genetic Loci Humans Male Polymorphism, Single Nucleotide