A novel deletion in the FTL gene causes hereditary hyperferritinemia cataract syndrome (HHCS) by alteration of the transcription start site

dc.contributor.authorBurdon, Kathryn Penelope
dc.contributor.authorSharma, Shiwani
dc.contributor.authorMackey, David A
dc.contributor.authorDimasi, David Paul
dc.contributor.authorCraig, Jamie E
dc.contributor.authorChen, Celia Shin Wen
dc.date.accessioned2010-07-27T05:52:50Z
dc.date.available2010-07-27T05:52:50Z
dc.date.issued2007en
dc.identifier.citationBurdon, K.P., Sharma, S., Chen, C.S., Mackey, D.A., Dimasi, D.P., & Craig, J., 2007. A novel deletion in the FTL gene causes hereditary hyperferritinemia cataract syndrome (HHCS) by alteration of the transcription start site. Human Mutation, 28(7), 742-751.en
dc.identifier.doihttps://doi.org/10.1002/humu.9501en
dc.identifier.issn1059-7794en
dc.identifier.rmid2006005914en
dc.identifier.urihttp://hdl.handle.net/2328/9257
dc.subject.forgroup0604 Geneticsen
dc.subject.forgroup1103 Clinical Sciencesen
dc.subject.forgroup1113 Ophthalmology and Optometryen
dc.titleA novel deletion in the FTL gene causes hereditary hyperferritinemia cataract syndrome (HHCS) by alteration of the transcription start siteen
dc.typeArticleen
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