A novel mutation in the Connexin 46 Gene causes autosomal dominant congenital cataract with incomplete penetrance

Kathryn Burdon, M Wirth, David Mackey, I Russell-Eggit, Jamie Craig, J Elder, J Dickinson, Michele Sale

    Research output: Contribution to journalArticle

    48 Citations (Scopus)
    Original languageEnglish
    Number of pages4
    JournalJournal of Medical Genetics
    Volume41
    Issue number8
    Publication statusPublished - 2004

    Cite this

    Burdon, K., Wirth, M., Mackey, D., Russell-Eggit, I., Craig, J., Elder, J., Dickinson, J., & Sale, M. (2004). A novel mutation in the Connexin 46 Gene causes autosomal dominant congenital cataract with incomplete penetrance. Journal of Medical Genetics, 41(8).