Investigation of crystallin genes in familial cataract, and report of two disease associated mutations

dc.contributor.author Mackay, D A
dc.contributor.author Craig, Jamie E
dc.contributor.author Russell-Eggit, Isabelle M
dc.contributor.author Wirth, M Gabriela
dc.contributor.author Dickinson, Joanne L
dc.contributor.author Elder, James E
dc.contributor.author Burdon, Kathryn Penelope
dc.date.accessioned 2010-07-27T06:20:28Z
dc.date.available 2010-07-27T06:20:28Z
dc.date.issued 2004 en_US
dc.description.note BRITISH MED ASSOC HOUSE, TAVISTOCK SQUARE, LONDON, ENGLAND, WC1H 9JR en
dc.identifier.citation Burdon, K.P., Wirth, M., Mackay, D., Russell-Eggit, I M, Craig, J., Elder, J.E., & Dickinson, J.L., 2004. Investigation of crystallin genes in familial cataract, and report of two disease associated mutations. British Journal of Ophthalmology, 88(1), 79-83. en
dc.identifier.doi https://doi.org/10.1136/bjo.88.1.79 en
dc.identifier.issn 0007-1161 en_US
dc.identifier.rmid 2004054729 en_US
dc.identifier.uri http://hdl.handle.net/2328/11237
dc.subject.forgroup 1113 Ophthalmology and Optometry en_US
dc.subject.forgroup 1103 Clinical Sciences en_US
dc.subject.forgroup 1117 Public Health and Health Services en_US
dc.title Investigation of crystallin genes in familial cataract, and report of two disease associated mutations en_US
dc.type Article en_US
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