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Recessive RHO mutation E150K and SAMD7 regulatory variants in a consanguineous family with retinitis pigmentosa

Kristof Van Schil UGent, Marcus Karlstetter, Alexander Aslanidis, Bart Leroy UGent, Frauke Coppieters, Fanny Depasse, Thomas Langmann and Elfride De Baere UGent (2015) EUROPEAN JOURNAL OF HUMAN GENETICS. 23(suppl. 1). p.83-83
Please use this url to cite or link to this publication:
author
organization
year
type
conference (poster)
publication status
published
subject
in
EUROPEAN JOURNAL OF HUMAN GENETICS
Eur. J. Hum. Genet.
volume
23
issue
suppl. 1
article number
abstract PS02.53
pages
83 - 83
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
8555687
handle
http://hdl.handle.net/1854/LU-8555687
alternative location
https://www.eshg.org/fileadmin/www.eshg.org/conferences/2015/downloads/ESHG2015_Abstracts_May_19.pdf
date created
2018-03-14 16:26:05
date last changed
2018-05-17 08:01:43
@inproceedings{8555687,
  articleno    = {abstract PS02.53},
  author       = {Van Schil, Kristof and Karlstetter, Marcus and Aslanidis, Alexander and Leroy, Bart and Coppieters, Frauke and Depasse, Fanny and Langmann, Thomas and De Baere, Elfride},
  booktitle    = {EUROPEAN JOURNAL OF HUMAN GENETICS},
  issn         = {1018-4813},
  language     = {eng},
  location     = {Glasgow, Scotland, UK},
  number       = {suppl. 1},
  pages        = {abstract PS02.53:83--abstract PS02.53:83},
  title        = {Recessive RHO mutation E150K and SAMD7 regulatory variants in a consanguineous family with retinitis pigmentosa},
  url          = {https://www.eshg.org/fileadmin/www.eshg.org/conferences/2015/downloads/ESHG2015\_Abstracts\_May\_19.pdf},
  volume       = {23},
  year         = {2015},
}

Chicago
Van Schil, Kristof, Marcus Karlstetter, Alexander Aslanidis, Bart Leroy, Frauke Coppieters, Fanny Depasse, Thomas Langmann, and Elfride De Baere. 2015. “Recessive RHO Mutation E150K and SAMD7 Regulatory Variants in a Consanguineous Family with Retinitis Pigmentosa.” In European Journal of Human Genetics, 23:83–83.
APA
Van Schil, K., Karlstetter, M., Aslanidis, A., Leroy, B., Coppieters, F., Depasse, F., Langmann, T., et al. (2015). Recessive RHO mutation E150K and SAMD7 regulatory variants in a consanguineous family with retinitis pigmentosa. EUROPEAN JOURNAL OF HUMAN GENETICS (Vol. 23, pp. 83–83). Presented at the European Human Genetics Conference 2015 (ESHG 2015).
Vancouver
1.
Van Schil K, Karlstetter M, Aslanidis A, Leroy B, Coppieters F, Depasse F, et al. Recessive RHO mutation E150K and SAMD7 regulatory variants in a consanguineous family with retinitis pigmentosa. EUROPEAN JOURNAL OF HUMAN GENETICS. 2015. p. 83–83.
MLA
Van Schil, Kristof, Marcus Karlstetter, Alexander Aslanidis, et al. “Recessive RHO Mutation E150K and SAMD7 Regulatory Variants in a Consanguineous Family with Retinitis Pigmentosa.” European Journal of Human Genetics. Vol. 23. 2015. 83–83. Print.