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Regulatory mutations in the 5'UTR of NMNAT1, encoding the nuclear isoform of nicotinamide nucleotide adenylyltransferase 1, cause Leber Congenital Amaurosis

Frauke Coppieters, Annelot Baert, Miriam Bauwens UGent, Caroline Van Cauwenbergh UGent, Sarah De Jaegere, Thomy de Ravel, Françoise Meire, Nouha Abdelmoula Bouayed, Lina Florentin-Arar, Bart Leroy UGent, et al. (2012) American Society of Human Genetics, 62nd Annual meeting, Abstracts.
Please use this url to cite or link to this publication:
author
organization
year
type
conference (meetingAbstract)
publication status
published
subject
keyword
Genetics, mutations
in
American Society of Human Genetics, 62nd Annual meeting, Abstracts
conference name
62nd Annual meeting of the American Society of Human Genetics (ASHG)
conference location
San Francisco, CA, USA
conference start
2012-11-06
conference end
2012-11-10
language
English
UGent publication?
yes
classification
C3
id
8119454
handle
http://hdl.handle.net/1854/LU-8119454
date created
2016-10-19 00:46:27
date last changed
2018-05-17 08:40:13
@inproceedings{8119454,
  author       = {Coppieters, Frauke and Baert, Annelot and Bauwens, Miriam and Van Cauwenbergh, Caroline and De Jaegere, Sarah and de Ravel, Thomy and Meire, Fran\c{c}oise and Bouayed, Nouha Abdelmoula and Florentin-Arar, Lina and Leroy, Bart and De Baere, Elfride},
  booktitle    = {American Society of Human Genetics, 62nd Annual meeting, Abstracts},
  keyword      = {Genetics,mutations},
  language     = {eng},
  location     = {San Francisco, CA, USA},
  title        = {Regulatory mutations in the 5'UTR of NMNAT1, encoding the nuclear isoform of nicotinamide nucleotide adenylyltransferase 1, cause Leber Congenital Amaurosis},
  year         = {2012},
}

Chicago
Coppieters, Frauke, Annelot Baert, Miriam Bauwens, Caroline Van Cauwenbergh, Sarah De Jaegere, Thomy de Ravel, Françoise Meire, et al. 2012. “Regulatory Mutations in the 5’UTR of NMNAT1, Encoding the Nuclear Isoform of Nicotinamide Nucleotide Adenylyltransferase 1, Cause Leber Congenital Amaurosis.” In American Society of Human Genetics, 62nd Annual Meeting, Abstracts.
APA
Coppieters, F., Baert, A., Bauwens, M., Van Cauwenbergh, C., De Jaegere, S., de Ravel, T., Meire, F., et al. (2012). Regulatory mutations in the 5’UTR of NMNAT1, encoding the nuclear isoform of nicotinamide nucleotide adenylyltransferase 1, cause Leber Congenital Amaurosis. American Society of Human Genetics, 62nd Annual meeting, Abstracts. Presented at the 62nd Annual meeting of the American Society of Human Genetics (ASHG).
Vancouver
1.
Coppieters F, Baert A, Bauwens M, Van Cauwenbergh C, De Jaegere S, de Ravel T, et al. Regulatory mutations in the 5’UTR of NMNAT1, encoding the nuclear isoform of nicotinamide nucleotide adenylyltransferase 1, cause Leber Congenital Amaurosis. American Society of Human Genetics, 62nd Annual meeting, Abstracts. 2012.
MLA
Coppieters, Frauke, Annelot Baert, Miriam Bauwens, et al. “Regulatory Mutations in the 5’UTR of NMNAT1, Encoding the Nuclear Isoform of Nicotinamide Nucleotide Adenylyltransferase 1, Cause Leber Congenital Amaurosis.” American Society of Human Genetics, 62nd Annual Meeting, Abstracts. 2012. Print.