Academic Bibliography

Search 200 years of publications by Ghent University researchers.

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Your filters: cql: author="Pécheux, Lucie" or (type exact bookEditor and editor="Pécheux, Lucie")

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- Conference Paper
- C3
Novel non-coding homozygous mutation 'Ghent +49A>G' in the iron-responsive element of L-ferritin causes hereditary hyperferritinaemia-cataract syndrome

Stijn Van de Sompele (UGent) , Audrey Meunier, Lucie Pécheux and Elfride De Baere (UGent)

(2017) Belgian Society for Human Genetics, 17th Annual meeting, Abstracts.
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- Conference Paper
- C3
Novel non-coding homozygous mutation 'Ghent +49A>G' in the iron-responsive element of L-ferritin causes hereditary hyperferritinaemia-cataract syndrome

Stijn Van de Sompele (UGent) , Audrey Meunier, Lucie Pécheux and Elfride De Baere (UGent)

(2017) Science Day, Faculty of Medicine and Health Science, Ghent University, Abstracts.
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- Journal Article
- A1
- open access
Functional characterization of a novel non-coding mutation 'Ghent +49A>G' in the iron-responsive element of L-ferritin causing hereditary hyperferritinaemia-cataract syndrome

Stijn Van de Sompele (UGent) , Lucie Pécheux, Jorge Couso, Audrey Meunier, Mayka Sanchez and Elfride De Baere (UGent)

(2017) SCIENTIFIC REPORTS. 7.