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Please use this identifier to cite or link to this item: http://hdl.handle.net/2328/9257

Title: A novel deletion in the FTL gene causes hereditary hyperferritinemia cataract syndrome (HHCS) by alteration of the transcription start site
Authors: Burdon, Kathryn Penelope
Sharma, Shiwani
Mackey, David A
Dimasi, David Paul
Craig, Jamie E
Chen, Celia S
Issue Date: 2007
Citation: Burdon, 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.
URI: http://hdl.handle.net/2328/9257
ISSN: 1059-7794
Appears in Collections:0604 - Genetics
1113 - Ophthalmology and Optometry
0604 - Genetics

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