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Online mutation report
A novel mutation in the Connexin 46 gene causes autosomal dominant congenital cataract with incomplete penetrance

https://doi.org/10.1136/jmg.2004.018333

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    Footnotes

    • Grant support for this project was received from the Ophthalmic Research Institute of Australia, the Jack Brockhoff Foundation, and the Royal Hobart Hospital Research Foundation.

    • Conflict of interest: none declared.

    Linked Articles

    • Correction
      CORRECTION
      BMJ Publishing Group Ltd
      Journal of Medical Genetics 2005; 42 288-288 Published Online First: 02 Mar 2005. doi: 10.1136/jmg.2005.18333corr1
    • Correction
      Correction
      BMJ Publishing Group Ltd
      Journal of Medical Genetics 2008; 45 256-256 Published Online First: 01 Apr 2008.