A novel deletion in the FTL gene causes hereditary hyperferritinemia cataract syndrome (HHCS) by alteration of the transcription start site
No Thumbnail Available
Date
2007
Authors
Burdon, Kathryn Penelope
Sharma, Shiwani
Mackey, David A
Dimasi, David Paul
Craig, Jamie E
Chen, Celia Shin Wen
Journal Title
Journal ISSN
Volume Title
Publisher
Rights
Rights Holder
Abstract
Description
Keywords
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.