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Audiological Evaluation of Affected Members from a Dutch DFNA8/12 (TECTA) Family
In DFNA8/12, an autosomal dominantly inherited type of nonsyndromic hearing impairment, the TECTA gene mutation causes a defect in the structure of the tectorial membrane in the inner ear. Because DFNA8/12 affects the tectorial membrane, patients with DFNA8/12 may show specific audiometric character...
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| Main Authors: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Springer-Verlag
2006
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2538417/ https://ncbi.nlm.nih.gov/pubmed/17136632 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s10162-006-0060-9 |
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