Advanced search
Add to list

Isolated and syndromic retinal dystrophy caused by biallelic mutations in RCBTB1, implicated in ubiquitination.

Author
Organization

Citation

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

MLA
Ascari, Giulia et al. “Isolated and Syndromic Retinal Dystrophy Caused by Biallelic Mutations in RCBTB1, Implicated in Ubiquitination.” Pro Retina, Research Colloquium, Abstracts. 2016. Print.
APA
Ascari, G., Coppieters, F., Dannhausen, K., Karlstetter, M., Nikopoulos, K., Xu, M., Bauwens, M., et al. (2016). Isolated and syndromic retinal dystrophy caused by biallelic mutations in RCBTB1, implicated in ubiquitination. Pro Retina, Research colloquium, Abstracts. Presented at the Pro Retina Research colloquium 2016.
Chicago author-date
Ascari, Giulia, Frauke Coppieters, K Dannhausen, M Karlstetter, K Nikopoulos, M Xu, Miriam Bauwens, et al. 2016. “Isolated and Syndromic Retinal Dystrophy Caused by Biallelic Mutations in RCBTB1, Implicated in Ubiquitination.” In Pro Retina, Research Colloquium, Abstracts.
Chicago author-date (all authors)
Ascari, Giulia, Frauke Coppieters, K Dannhausen, M Karlstetter, K Nikopoulos, M Xu, Miriam Bauwens, Marieke De Bruyne, Thalia Van Laethem, F Meire, R Chen, T Langmann, C Rivolta, CP Hamel, Bart Leroy, and Elfride De Baere. 2016. “Isolated and Syndromic Retinal Dystrophy Caused by Biallelic Mutations in RCBTB1, Implicated in Ubiquitination.” In Pro Retina, Research Colloquium, Abstracts.
Vancouver
1.
Ascari G, Coppieters F, Dannhausen K, Karlstetter M, Nikopoulos K, Xu M, et al. Isolated and syndromic retinal dystrophy caused by biallelic mutations in RCBTB1, implicated in ubiquitination. Pro Retina, Research colloquium, Abstracts. 2016.
IEEE
[1]
G. Ascari et al., “Isolated and syndromic retinal dystrophy caused by biallelic mutations in RCBTB1, implicated in ubiquitination.,” in Pro Retina, Research colloquium, Abstracts, Potsdam, Germany , 2016.
@inproceedings{8589100,
  author       = {Ascari, Giulia and Coppieters, Frauke and Dannhausen, K and Karlstetter, M and Nikopoulos, K and Xu, M and Bauwens, Miriam and De Bruyne, Marieke and Van Laethem, Thalia and Meire, F and Chen, R and Langmann, T and Rivolta, C and Hamel, CP and Leroy, Bart and De Baere, Elfride},
  booktitle    = {Pro Retina, Research colloquium, Abstracts},
  language     = {eng},
  location     = {Potsdam, Germany },
  title        = {Isolated and syndromic retinal dystrophy caused by biallelic mutations in RCBTB1, implicated in ubiquitination.},
  year         = {2016},
}