Functional evaluation of GJB2 variants in nonsyndromic hearing loss. [electronic resource]
- Molecular medicine (Cambridge, Mass.)
- 550-6 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
1528-3658
10.2119/molmed.2010.00183 doi
Alleles Asian People Cell Line Connexin 26 Connexins--genetics Gap Junctions--genetics Genotype Haplotypes--genetics Hearing Loss--genetics Humans Linkage Disequilibrium--genetics Polymorphism, Genetic--genetics