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Orphanet Journal of Rare Diseases logoLink to Orphanet Journal of Rare Diseases
. 2013 Aug 14;8:120. doi: 10.1186/1750-1172-8-120

Correction: COG5-CDG: expanding the clinical spectrum

Daisy Rymen 1,2, Liesbeth Keldermans 1, Valérie Race 1, Luc Régal 2, Nicolas Deconinck 3, Carlo Dionisi-Vici 4, Cheuk-wing Fung 5, Luisa Sturiale 6, Claire Rosnoblet 7, François Foulquier 7, Gert Matthijs 1, Jaak Jaeken 2,
PMCID: PMC3750997

Correction

After the publication of this work [1] it was brought to the authors attention that the appropriate ethical approval and patient consent was not stated in the manuscript. We regret any inconvenience that this may have caused. The correct statement is given below:

Following approval from the institutional ethics committee, the family of all patients in this study provided written consent to participate in this study, along with consent to publish their clinical details and photographs.

Contributor Information

Daisy Rymen, Email: daisy.rymen@uzleuven.be.

Liesbeth Keldermans, Email: liesbeth.keldermans@med.kuleuven.be.

Valérie Race, Email: valerie.race@uzleuven.be.

Luc Régal, Email: luc.regal@uzleuven.be.

Nicolas Deconinck, Email: nicolas.deconinck@huderf.be.

Carlo Dionisi-Vici, Email: dionisi@opbg.net.

Cheuk-wing Fung, Email: fcw120gm@hkstar.com.

Luisa Sturiale, Email: luisella.sturiale@cnr.it.

Claire Rosnoblet, Email: claire.rosnoblet@univ-lille1.fr.

François Foulquier, Email: francois.foulquier@univ-lille1.fr.

Gert Matthijs, Email: gert.matthijs@uzleuven.be.

Jaak Jaeken, Email: jaak.jaeken@uzleuven.be.

References

  1. Rymen. et al. COG5-CDG: expanding the clinical spectrum. Orphanet J Rare Dis. 2012;7:94. doi: 10.1186/1750-1172-7-94. [DOI] [PMC free article] [PubMed] [Google Scholar]

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