DFNA8/12 caused by TECTA mutations is the most identified subtype of nonsyndromic autosomal dominant hearing loss.
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| Description | scientific article published on 7 June 2011 |
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author: Matías Morín Michael S. Hildebrand Ignacio del Castillo Isabelle Schrauwen Carmelo Morales-Angulo Adam P. DeLuca Hannie Kremer Katherine L Lachlan Guy Van Camp Richard J Smith |
| Publication date | June 7, 2011 |
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