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A novel mutation in the Connexin 46 gene causes autosomal dominant congenital cataract with incomplete penetrance
  1. Correspondence to:
 Dr M M Sale
 Center for Human Genomics, Wake Forest University School of Medicine, Medical Center Blvd, Winston-Salem, NC 27157, USA; msalewfubmc.edu
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Citation

Burdon KP, Wirth MG, Mackey DA, et al
A novel mutation in the Connexin 46 gene causes autosomal dominant congenital cataract with incomplete penetrance

Publication history

  • Received March 5, 2004
  • Accepted March 10, 2004
  • First published July 30, 2004.
Online issue publication 
April 27, 2016

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