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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]
Data TypeValue
Type of ResearchApplied Research
Research DivisionBiomedical and Clinical Sciences
Research GroupOphthalmology and optometry
Research FieldOphthalmology
Research Objective DivisionHealth
Research Objective GroupClinical health
Research Objective FieldClinical health not elsewhere classified
Visit Item on eCitehttp://ecite.utas.edu.au/30836
Digital Object Identifierdoi:10.1136/jmg.2004.018333
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Number of Times Cited50