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A homozygous B3GAT3 mutation causes a multisystemic cutis laxa-like syndrome, expanding the phenotype of linkeropathies

Brecht Guillemyn (UGent) , Tim Van Damme (UGent) , Wouter Steyaert (UGent) , Delfien Syx (UGent) , Paul Coucke (UGent) , Anne De Paepe (UGent) , Sofie Symoens (UGent) , Sheela Nampoothiri and Fransiska Malfait (UGent)
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Chicago
Guillemyn, Brecht, Tim Van Damme, Wouter Steyaert, Delfien Syx, Paul Coucke, Anne De Paepe, Sofie Symoens, Sheela Nampoothiri, and Fransiska Malfait. 2016. “A Homozygous B3GAT3 Mutation Causes a Multisystemic Cutis Laxa-like Syndrome, Expanding the Phenotype of Linkeropathies.” In European Human Genetics Conference, Abstracts.
APA
Guillemyn, B., Van Damme, T., Steyaert, W., Syx, D., Coucke, P., De Paepe, A., Symoens, S., et al. (2016). A homozygous B3GAT3 mutation causes a multisystemic cutis laxa-like syndrome, expanding the phenotype of linkeropathies. European Human Genetics conference, Abstracts. Presented at the European Human Genetics Conference 2016 (ESHG 2016).
Vancouver
1.
Guillemyn B, Van Damme T, Steyaert W, Syx D, Coucke P, De Paepe A, et al. A homozygous B3GAT3 mutation causes a multisystemic cutis laxa-like syndrome, expanding the phenotype of linkeropathies. European Human Genetics conference, Abstracts. 2016.
MLA
Guillemyn, Brecht, Tim Van Damme, Wouter Steyaert, et al. “A Homozygous B3GAT3 Mutation Causes a Multisystemic Cutis Laxa-like Syndrome, Expanding the Phenotype of Linkeropathies.” European Human Genetics Conference, Abstracts. 2016. Print.
@inproceedings{8513530,
  author       = {Guillemyn, Brecht and Van Damme, Tim and Steyaert, Wouter and Syx, Delfien and Coucke, Paul and De Paepe, Anne and Symoens, Sofie and Nampoothiri, Sheela and Malfait, Fransiska},
  booktitle    = {European Human Genetics conference, Abstracts},
  language     = {eng},
  location     = {Barcelona, Spain},
  title        = {A homozygous B3GAT3 mutation causes a multisystemic cutis laxa-like syndrome, expanding the phenotype of linkeropathies},
  year         = {2016},
}