Advanced search

A mutant ATP6V1E1 zebrafish model recapitulates the human cutis laxa syndrome

Lore Pottie (UGent) , Patrick Sips (UGent) , Paul Coucke (UGent) and Bert Callewaert (UGent)
Author
Organization

Citation

Please use this url to cite or link to this publication:

Chicago
Pottie, Lore, Patrick Sips, Paul Coucke, and Bert Callewaert. 2018. “A Mutant ATP6V1E1 Zebrafish Model Recapitulates the Human Cutis Laxa Syndrome.” In Belgian Society for Human Genetics, 18th Annual Meeting, Abstracts.
APA
Pottie, L., Sips, P., Coucke, P., & Callewaert, B. (2018). A mutant ATP6V1E1 zebrafish model recapitulates the human cutis laxa syndrome. Belgian Society for Human Genetics, 18th Annual meeting, Abstracts. Presented at the 18th Annual BeSHG meeting: The epigenome in development and disease.
Vancouver
1.
Pottie L, Sips P, Coucke P, Callewaert B. A mutant ATP6V1E1 zebrafish model recapitulates the human cutis laxa syndrome. Belgian Society for Human Genetics, 18th Annual meeting, Abstracts. 2018.
MLA
Pottie, Lore, Patrick Sips, Paul Coucke, et al. “A Mutant ATP6V1E1 Zebrafish Model Recapitulates the Human Cutis Laxa Syndrome.” Belgian Society for Human Genetics, 18th Annual Meeting, Abstracts. 2018. Print.
@inproceedings{8561335,
  author       = {Pottie, Lore and Sips, Patrick and Coucke, Paul and Callewaert, Bert},
  booktitle    = {Belgian Society for Human Genetics, 18th Annual meeting, Abstracts},
  language     = {eng},
  location     = {Ghent, Belgium},
  title        = {A mutant ATP6V1E1 zebrafish model recapitulates the human cutis laxa syndrome},
  year         = {2018},
}