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

Da, Mackey; Wirth, Mg G.; Russell-Eggitt, I. M.; Craig, J. E.; Elder, J. E.; Dickinson, J. L.; Sale, M. M.; Burdon, Kp P.

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BMJ Publishing Group, Journal of Medical Genetics, 8(41), p. e106-e106, 2004

DOI: 10.1136/jmg.2004.018333

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

Journal article published in 2004 by Mackey Da, Mg G. Wirth, I. M. Russell-Eggitt, J. E. Craig, J. E. Elder, J. L. Dickinson, M. M. Sale, Kp P. Burdon

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