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

    Burdon, Kathryn Penelope; Sharma, Shiwani; Mackey, David A; Dimasi, David Paul; Craig, Jamie E; Chen, Celia Shin Wen (2007)

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    AuthorBurdon, Kathryn Penelope (1)
    Chen, Celia Shin Wen (1)
    Craig, Jamie E (1)
    Dimasi, David Paul (1)
    Mackey, David A (1)
    Sharma, Shiwani (1)Subject0604 Genetics (1)
    1103 Clinical Sciences (1)
    1113 Ophthalmology and Optometry (1)
    ... View MoreDate Issued2007 (1)

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