POSTSCRIPT
Correction
Correction
| The first 100% of the full text of this article appears below. |
Burdon KP, Wirth MG, Mackey DA, Russell-Eggitt IM, Craig JE, Elder JE, Dickinson JL, Sale MM. A novel mutation in the Connexin 46 gene causes autosomal dominant congenital cataract with incomplete penetrance. J Med Genet 2004;41:e106.
The authors apologise for an error in figure 2. Individuals V:1 and IV:12 should be marked as affected. Both have ophthalmologist confirmed cataract. The corrected figure 2 is shown here.
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