A novel mutation in the Connexin 46 Gene causes
autosomal dominant congenital cataract with incomplete penetrance
A novel mutation in the Connexin 46 Gene causes
autosomal dominant congenital cataract with incomplete penetrance
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Date
2004
Authors
Craig, Jamie E
Sale, Michele M
Mackey, David A
Russell-Eggit, Isabelle M
Wirth, M Gabriela
Dickinson, Joanne L
Elder, James E
Burdon, Kathryn Penelope
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Citation
Burdon, K.P., Wirth, M., Mackey, D.A.,
Russell-Eggit, I M, Craig, J., Elder, J.E., Dickinson, J.L., & Sale, M.M., 2004. A
novel mutation in the Connexin 46 Gene causes autosomal dominant congenital cataract
with incomplete penetrance. Journal of Medical Genetics, 41(8).