| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 4107512 | Brazilian Journal of Otorhinolaryngology | 2006 | 4 Pages |
Abstract
The data confirm the high prevalence of the 35delG mutation in nonsyndromic bilateral profound sensorineural hearing loss. It was also possible to diagnose the cause of hearing loss as genetic in a significant percentage of patients. That stresses the importance of the molecular investigation in those cases formerly classified as idiopathic.
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Authors
Raquel Bernardes, Silvana Bortoncello, Thalita Vitachi Christiani, Edi Lúcia Sartorato, Rodrigo César e Silva, Paulo R. Cantanhede Porto,