Transgenic expression of a dominant-negative connexin26 causes degeneration of the organ of Corti and non-syndromic deafness
Work
Year: 2003
Type: article
Abstract: Hereditary deafness affects about 1 in 2000 children and mutations in the GJB2 gene are the major cause in various ethnic groups. GJB2 encodes connexin26, a putative channel component in cochlear gap ... more
Source: Human Molecular Genetics
Institutions Tohoku University, Tohoku Medical Megabank Organization
Cites: 25
Cited by: 157
Related to: 10
FWCI: 3.547
Citation percentile (by year/subfield): 99.91
Subfield: Sensory Systems
Field: Neuroscience
Domain: Life Sciences
Sustainable Development Goal Good health and well-being
Open Access status: bronze