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dc.contributor.authorSouzeau, Emmanuelle
dc.contributor.authorBurdon, Kathryn Penelope
dc.contributor.authorDubowsky, Andrew
dc.contributor.authorGrist, S
dc.contributor.authorUsher, Bronwyn
dc.contributor.authorFitzgerald, Jude T
dc.contributor.authorCrawford, April
dc.contributor.authorHewitt, Alex W
dc.contributor.authorGoldberg, Ivan
dc.contributor.authorMills, Richard Arthur
dc.contributor.authorRuddle, Jonathan B
dc.contributor.authorLanders, John
dc.contributor.authorMackey, David A
dc.contributor.authorCraig, Jamie E
dc.identifier.citationSouzeau, E., Burdon, K.P., Dubowsky, A., Grist, S., Usher, B., Fitzgerald, J.T., Crawford, A., Hewitt, A.W., Goldberg, I., Mills, R.A., Ruddle, J.B., Landers, J., Mackey, D.A. and Craig, J.E., 2013. Higher prevalence of Myocilin mutations in advanced glaucoma in comparison with less advanced disease in an Australasian disease registry. Ophthalmology, 120(6), 1135-1143.en
dc.descriptionThis article appeared in a journal published by Elsevier Ltd. Under Elsevier's copyright, mandated authors are not permitted to make work available in an institutional repository.en
dc.description.abstractThe prevalence of Myocilin mutations in glaucoma cases with severe visual field loss is significantly greater than in nonadvanced glaucoma patients. Myocilin screening in phenotypically selected cases can have a much higher yield than in previous unselected series. Identifying individuals who have Myocilin mutations provides an opportunity to screen at-risk clinically unaffected relatives and to reduce glaucoma blindness through early management and intervention.en
dc.description.sponsorshipAustralian National Health & Medical Research Councilen
dc.rightsCopyright 2012 American Academy of Ophthalmology. Published by Elsevier Inc. All rights reserved.en
dc.titleHigher prevalence of Myocilin mutations in advanced glaucoma in comparison with less advanced disease in an Australasian disease registryen
dc.rights.holderElsevier, Ltd.en

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