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 journal › Article › peer-review

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Cite this

@article{095f848c02674eb78374a6d3b4976d0e,

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

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

year = "2004",

language = "English",

volume = "41",

journal = "Journal of Medical Genetics",

issn = "0022-2593",

publisher = "BMJ Publishing Group",

number = "8",

}

TY - JOUR

T1 - A novel mutation in the Connexin 46 Gene causes autosomal dominant congenital cataract with incomplete penetrance

AU - Burdon, Kathryn

AU - Wirth, M

AU - Mackey, David

AU - Russell-Eggit, I

AU - Craig, Jamie

AU - Elder, J

AU - Dickinson, J

AU - Sale, Michele

PY - 2004

Y1 - 2004

M3 - Article

SN - 0022-2593

VL - 41

JO - Journal of Medical Genetics

JF - Journal of Medical Genetics

IS - 8

ER -