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Knockdown and knockout zebrafish models for the β4GalT7-deficient type of Ehlers-Danlos syndrome reveal distinctive and overlapping phenotypic features

Sarah Delbaere (UGent) , Tim Van Damme (UGent) , Delfien Syx (UGent) , Sofie Symoens (UGent) , Andy Willaert (UGent) and Fransiska Malfait (UGent)
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Chicago
Delbaere, Sarah, Tim Van Damme, Delfien Syx, Sofie Symoens, Andy Willaert, and Fransiska Malfait. 2018. “Knockdown and Knockout Zebrafish Models for the β4GalT7-deficient Type of Ehlers-Danlos Syndrome Reveal Distinctive and Overlapping Phenotypic Features.” In Proteoglycans in Homeostasis and Disease, Gordon Research Conference, Abstracts.
APA
Delbaere, S., Van Damme, T., Syx, D., Symoens, S., Willaert, A., & Malfait, F. (2018). Knockdown and knockout zebrafish models for the β4GalT7-deficient type of Ehlers-Danlos syndrome reveal distinctive and overlapping phenotypic features. Proteoglycans in Homeostasis and Disease, Gordon research conference, Abstracts. Presented at the Gordon research conference on Proteoglycans in Homeostasis and Disease: Cracking the PG code.
Vancouver
1.
Delbaere S, Van Damme T, Syx D, Symoens S, Willaert A, Malfait F. Knockdown and knockout zebrafish models for the β4GalT7-deficient type of Ehlers-Danlos syndrome reveal distinctive and overlapping phenotypic features. Proteoglycans in Homeostasis and Disease, Gordon research conference, Abstracts. 2018.
MLA
Delbaere, Sarah et al. “Knockdown and Knockout Zebrafish Models for the β4GalT7-deficient Type of Ehlers-Danlos Syndrome Reveal Distinctive and Overlapping Phenotypic Features.” Proteoglycans in Homeostasis and Disease, Gordon Research Conference, Abstracts. 2018. Print.
@inproceedings{8602841,
  author       = {Delbaere, Sarah and Van Damme, Tim and Syx, Delfien and Symoens, Sofie and Willaert, Andy and Malfait, Fransiska},
  booktitle    = {Proteoglycans in Homeostasis and Disease, Gordon research conference, Abstracts},
  language     = {eng},
  location     = {Andover, NH, USA},
  title        = {Knockdown and knockout zebrafish models for the β4GalT7-deficient type of Ehlers-Danlos syndrome reveal distinctive and overlapping phenotypic features},
  year         = {2018},
}