A novel deletion in the FTL gene causes hereditary hyperferritinemia cataract syndrome (HHCS) by alteration of the transcription start site
A novel deletion in the FTL gene causes hereditary hyperferritinemia cataract syndrome (HHCS) by alteration of the transcription start site
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Date
2007
Authors
Burdon, Kathryn Penelope
Sharma, Shiwani
Mackey, David A
Dimasi, David Paul
Craig, Jamie E
Chen, Celia Shin Wen
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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.