A novel mutation in the Connexin 46 gene causes autosomal dominant congenital cataract with incomplete penetrance (Journal of Medical Genetics (2004) 41, (e106))

K. P. Burdon; M. G. Wirth; D. A. Mackey; I. M. Russell-Eggitt; J. E. Craig; J. E. Elder; J. L. Dickinson; M. M. Sale

doi:10.1136/jmg.2004.018333

A novel mutation in the Connexin 46 gene causes autosomal dominant congenital cataract with incomplete penetrance (Journal of Medical Genetics (2004) 41, (e106))

K. P. Burdon, M. G. Wirth, D. A. Mackey, I. M. Russell-Eggitt, J. E. Craig, J. E. Elder, J. L. Dickinson, M. M. Sale

Research output: Contribution to journal › Comment/debate

Original language	English
Pages (from-to)	256
Number of pages	1
Journal	Journal of Medical Genetics
Volume	45
Issue number	4
DOIs	https://doi.org/10.1136/jmg.2004.018333
Publication status	Published - 1 Apr 2008

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Burdon, K. P., Wirth, M. G., Mackey, D. A., Russell-Eggitt, I. M., Craig, J. E., Elder, J. E., Dickinson, J. L., & Sale, M. M. (2008). A novel mutation in the Connexin 46 gene causes autosomal dominant congenital cataract with incomplete penetrance (Journal of Medical Genetics (2004) 41, (e106)). Journal of Medical Genetics, 45(4), 256. https://doi.org/10.1136/jmg.2004.018333

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author = "Burdon, {K. P.} and Wirth, {M. G.} and Mackey, {D. A.} and Russell-Eggitt, {I. M.} and Craig, {J. E.} and Elder, {J. E.} and Dickinson, {J. L.} and Sale, {M. M.}",

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AU - Craig, J. E.

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AU - Dickinson, J. L.

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A novel mutation in the Connexin 46 gene causes autosomal dominant congenital cataract with incomplete penetrance (Journal of Medical Genetics (2004) 41, (e106))

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