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Novel non-coding homozygous mutation 'Ghent +49A>G' in the iron-responsive element of L-ferritin causes hereditary hyperferritinaemia-cataract syndrome

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Chicago
Van De Sompele, Stijn, Audrey Meunier, Lucie Pécheux, and Elfride De Baere. 2017. “Novel Non-coding Homozygous Mutation ‘Ghent +49A>G’ in the Iron-responsive Element of L-ferritin Causes Hereditary Hyperferritinaemia-cataract Syndrome.” In Science Day, Faculty of Medicine and Health Science, Ghent University, Abstracts.
APA
Van De Sompele, S., Meunier, A., Pécheux, L., & De Baere, E. (2017). Novel non-coding homozygous mutation “Ghent +49A>G” in the iron-responsive element of L-ferritin causes hereditary hyperferritinaemia-cataract syndrome. Science Day, Faculty of Medicine and Health Science, Ghent University, Abstracts. Presented at the Research Day of the Faculty of Medicine and Health Science, Ghent University.
Vancouver
1.
Van De Sompele S, Meunier A, Pécheux L, De Baere E. Novel non-coding homozygous mutation “Ghent +49A>G” in the iron-responsive element of L-ferritin causes hereditary hyperferritinaemia-cataract syndrome. Science Day, Faculty of Medicine and Health Science, Ghent University, Abstracts. 2017.
MLA
Van De Sompele, Stijn et al. “Novel Non-coding Homozygous Mutation ‘Ghent +49A>G’ in the Iron-responsive Element of L-ferritin Causes Hereditary Hyperferritinaemia-cataract Syndrome.” Science Day, Faculty of Medicine and Health Science, Ghent University, Abstracts. 2017. Print.
@inproceedings{8556176,
  author       = {Van De Sompele, Stijn and Meunier, Audrey and P{\'e}cheux, Lucie and De Baere, Elfride},
  booktitle    = {Science Day, Faculty of Medicine and Health Science, Ghent University, Abstracts},
  language     = {eng},
  location     = {Ghent, Belgium},
  title        = {Novel non-coding homozygous mutation 'Ghent +49A{\textrangle}G' in the iron-responsive element of L-ferritin causes hereditary hyperferritinaemia-cataract syndrome},
  year         = {2017},
}