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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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Autors principals: Plantinga, Rutger F., Cremers, Cor W.R.J., Huygen, Patrick L.M., Kunst, Henricus P.M., Bosman, Arjan J.
Format: Artigo
Idioma:Inglês
Publicat: Springer-Verlag 2006
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Accés en línia: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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