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A mutation in the gamma actin 1 (ACTG1) gene causes autosomal dominant hearing loss (DFNA20/26)
  1. Correspondence to:
 Dr H Kremer
 Department of Otorhinolaryngology, UMC Nijmegen, PO Box 9101, 6500 HB Nijmegen, Netherlands\|[semi]\|h.kremerantrg.umcn.nl
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Citation

van Wijk E, Krieger E, Kemperman MH, et al
A mutation in the gamma actin 1 (ACTG1) gene causes autosomal dominant hearing loss (DFNA20/26)

Publication history

  • Received July 12, 2003
  • Accepted September 5, 2003
  • First published December 18, 2003.
Online issue publication 
December 18, 2003

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