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Publication : Mutations in a novel isoform of TRIOBP that encodes a filamentous-actin binding protein are responsible for DFNB28 recessive nonsyndromic hearing loss.

First Author  Shahin H Year  2006
Journal  Am J Hum Genet Volume  78
Issue  1 Pages  144-52
PubMed ID  16385458 Mgi Id 
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