eCite Digital Repository

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

Citation

Burdon, KP and Wirth, MG and Mackey, DA and Russell-Eggitt, IM and Craig, JE and Elder, JE and Dickinson, JL and Sale, MM, A novel mutation in the Connexin 46 gene causes autosomal dominant congenital cataract with incomplete penetrance, Journal of Medical Genetics, 41, (8) pp. e106-109. ISSN 0022-2593 (2004) [Refereed Article]

DOI: doi:10.1136/jmg.2004.018333

Item Details

Item Type:Refereed Article
Research Division:Medical and Health Sciences
Research Group:Ophthalmology and Optometry
Research Field:Ophthalmology
Objective Division:Health
Objective Group:Clinical Health (Organs, Diseases and Abnormal Conditions)
Objective Field:Hearing, Vision, Speech and Their Disorders
Author:Burdon, KP (Associate Professor Kathryn Burdon)
Author:Mackey, DA (Professor David Mackey)
Author:Craig, JE (Mr Jamie Craig)
Author:Dickinson, JL (Associate Professor Joanne Dickinson)
Author:Sale, MM (Dr Michele Sale)
ID Code:30836
Year Published:2004
Web of Science® Times Cited:44
Deposited By:Medicine (Discipline)
Deposited On:2004-08-01
Last Modified:2011-11-08
Downloads:0

Repository Staff Only: item control page