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SF3B2, a novel candidate gene for autosomal dominant retinitis pigmentosa, encodes a component of the U2 small nuclear ribonucleoprotein

Caroline Van Cauwenbergh UGent, Marcus Karlstetter, Kris Vleminckx UGent, Gael Manes, Thomas Langmann, Christian Hamel, Bart Leroy UGent, Frauke Coppieters and Elfride De Baere UGent (2015) EUROPEAN JOURNAL OF HUMAN GENETICS. 23(suppl. 1). p.73-73
Please use this url to cite or link to this publication:
author
organization
year
type
conference (meetingAbstract)
publication status
published
subject
keyword
retinitis pigmentosa, genetics
in
EUROPEAN JOURNAL OF HUMAN GENETICS
Eur. J. Hum. Genet.
volume
23
issue
suppl. 1
article number
abstract PS02.05
pages
73 - 73
conference name
European Human Genetics Conference 2015 (ESHG 2015)
conference location
Glasgow, Scotland, UK
conference start
2015-06-06
conference end
2015-06-09
JCR category
GENETICS & HEREDITY
JCR impact factor
4.58 (2015)
JCR rank
30/165 (2015)
JCR quartile
1 (2015)
ISSN
1018-4813
language
English
UGent publication?
yes
classification
C3
id
8119490
handle
http://hdl.handle.net/1854/LU-8119490
alternative location
https://www.eshg.org/fileadmin/www.eshg.org/conferences/2015/downloads/ESHG2015_Abstracts_May_19.pdf
date created
2016-10-19 01:44:14
date last changed
2018-05-17 07:55:47
@inproceedings{8119490,
  articleno    = {abstract PS02.05},
  author       = {Van Cauwenbergh, Caroline and Karlstetter, Marcus and Vleminckx, Kris and Manes, Gael and Langmann, Thomas and Hamel, Christian and Leroy, Bart and Coppieters, Frauke and De Baere, Elfride},
  booktitle    = {EUROPEAN JOURNAL OF HUMAN GENETICS},
  issn         = {1018-4813},
  keyword      = {retinitis pigmentosa,genetics},
  language     = {eng},
  location     = {Glasgow, Scotland, UK},
  number       = {suppl. 1},
  pages        = {abstract PS02.05:73--abstract PS02.05:73},
  title        = {SF3B2, a novel candidate gene for autosomal dominant retinitis pigmentosa, encodes a component of the U2 small nuclear ribonucleoprotein},
  url          = {https://www.eshg.org/fileadmin/www.eshg.org/conferences/2015/downloads/ESHG2015\_Abstracts\_May\_19.pdf},
  volume       = {23},
  year         = {2015},
}

Chicago
Van Cauwenbergh, Caroline, Marcus Karlstetter, Kris Vleminckx, Gael Manes, Thomas Langmann, Christian Hamel, Bart Leroy, Frauke Coppieters, and Elfride De Baere. 2015. “SF3B2, a Novel Candidate Gene for Autosomal Dominant Retinitis Pigmentosa, Encodes a Component of the U2 Small Nuclear Ribonucleoprotein.” In European Journal of Human Genetics, 23:73–73.
APA
Van Cauwenbergh, C., Karlstetter, M., Vleminckx, K., Manes, G., Langmann, T., Hamel, C., Leroy, B., et al. (2015). SF3B2, a novel candidate gene for autosomal dominant retinitis pigmentosa, encodes a component of the U2 small nuclear ribonucleoprotein. EUROPEAN JOURNAL OF HUMAN GENETICS (Vol. 23, pp. 73–73). Presented at the European Human Genetics Conference 2015 (ESHG 2015).
Vancouver
1.
Van Cauwenbergh C, Karlstetter M, Vleminckx K, Manes G, Langmann T, Hamel C, et al. SF3B2, a novel candidate gene for autosomal dominant retinitis pigmentosa, encodes a component of the U2 small nuclear ribonucleoprotein. EUROPEAN JOURNAL OF HUMAN GENETICS. 2015. p. 73–73.
MLA
Van Cauwenbergh, Caroline, Marcus Karlstetter, Kris Vleminckx, et al. “SF3B2, a Novel Candidate Gene for Autosomal Dominant Retinitis Pigmentosa, Encodes a Component of the U2 Small Nuclear Ribonucleoprotein.” European Journal of Human Genetics. Vol. 23. 2015. 73–73. Print.