A novel deletion in the FTL gene causes hereditary hyperferritinemia cataract syndrome (HHCS) by alteration of the transcription start site. (Q53567971)
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scientific article published in July 2007
Language | Label | Description | Also known as |
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English | A novel deletion in the FTL gene causes hereditary hyperferritinemia cataract syndrome (HHCS) by alteration of the transcription start site. |
scientific article published in July 2007 |
Statements
A novel deletion in the FTL gene causes hereditary hyperferritinemia cataract syndrome (HHCS) by alteration of the transcription start site. (English)
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Jamie E Craig
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Kathryn P Burdon
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Shiwani Sharma
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Celia S Chen
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David P Dimasi
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David A Mackey
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1 July 2007
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28
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7
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742
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Identifiers
1 reference