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

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

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