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Nonsyndromic Deafness - Molecular Update
2009
The Open Biology Journal
In most cases, hearing loss is a disorder caused by both genetic and environmental factors. The molecular description of deafness has experienced remarkable progress in the last decade, and it is emerging from the use of contemporary methods of cell and molecular biology. Currently, through the application of clinical and molecular genetics it is possible to identify genes associated with inherited, nonsyndromic deafness, and balance dysfunctions of the human cochlea. This brief review provides
doi:10.2174/1874196700902010080
fatcat:h6w6yul42ffrdbsldmdbx252sy