Investigation of the prevalence of the myocilin Q368STOP mutation in Ugandan glaucoma patients

Michèle M. Sale Menzies Centre for Population Health Research, University of Tasmania,

Liesel M. FitzGerald Menzies Centre for Population Health Research, University of Tasmania,

Kenneth Kagame The Ruharo Eye Centre, Mbarara, Uganda, Africa,

Irmela Erdmann The Ruharo Eye Centre, Mbarara, Uganda, Africa,

Jamie E. Craig Centre for Eye Research Australia, Royal Victorian Eye and Ear Hospital, East Melbourne, Victoria, Australia, and

Joanne L. Dickinson Menzies Centre for Population Health Research, University of Tasmania,

Richard L. Cooper Tasmanian Eye Clinics, Hobart, Tasmania

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References

Fingert JH, Héon E, Liebmann J, Yamamoto T, Craig J, Rait J, Kawase K, Hoh S, Buys Y, Dickinson J, Hockey R, Williams-Lyn D, Trope G, Kitazawa Y, Ritch R, Mackey D, Alward W, Sheffield V, Stone E. Analysis of myocilin mutations in 1703 glaucoma patients from five different populations. Hum Mol Genet. 1999;8:899-9o5.
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Alward W, Fingert J, Coote M, Johnson T, Lerner F, Junqua D, Durcan F, McCartney P, Mackey D, Sheffield V, Stone E. Clinical features associated with mutations in the chromosome 1 open-angle glaucoma gene (GLCIA). N Engl J Med. 1998;338: 1022–1027.
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Baird P, Dickinson J, Craig JE, Mackey D. The Taal restriction enzyme provides a simple means to identify the Q3685T0P mutation of the myocilin gene in primary open angle glaucoma. Am J Ophthalmol. 2001;131:510–511.
PubMed Web of Science ®Google Scholar

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