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Exon 10b of the NF1 gene represents a mutational hotspot and harbors a recurrent missense mutation Y489C associated with aberrant splicing.

Ludwine Messiaen, T CALLENS, KJ ROUX, Geert Mortier, Anne De Paepe UGent, M ABRAMOWICZ, MA PERICAK-VANCE, JM VANCE and MR WALLACE (1999) GENETICS IN MEDICINE. 1(6). p.248-253
Please use this url to cite or link to this publication:
author
organization
year
type
journalArticle (original)
publication status
published
subject
journal title
GENETICS IN MEDICINE
Genet. Med.
volume
1
issue
6
pages
248-253 pages
Web of Science type
Article
Web of Science id
000084590600003
ISSN
1098-3600
language
English
UGent publication?
yes
classification
A1
id
115068
handle
http://hdl.handle.net/1854/LU-115068
date created
2004-01-14 13:35:00
date last changed
2016-12-19 15:36:49
@article{115068,
  author       = {Messiaen, Ludwine and CALLENS, T and ROUX, KJ and Mortier, Geert and De Paepe, Anne and ABRAMOWICZ, M and PERICAK-VANCE, MA and VANCE, JM and WALLACE, MR},
  issn         = {1098-3600},
  journal      = {GENETICS IN MEDICINE},
  language     = {eng},
  number       = {6},
  pages        = {248--253},
  title        = {Exon 10b of the NF1 gene represents a mutational hotspot and harbors a recurrent missense mutation Y489C associated with aberrant splicing.},
  volume       = {1},
  year         = {1999},
}

Chicago
Messiaen, Ludwine, T CALLENS, KJ ROUX, Geert Mortier, Anne De Paepe, M ABRAMOWICZ, MA PERICAK-VANCE, JM VANCE, and MR WALLACE. 1999. “Exon 10b of the NF1 Gene Represents a Mutational Hotspot and Harbors a Recurrent Missense Mutation Y489C Associated with Aberrant Splicing.” Genetics in Medicine 1 (6): 248–253.
APA
Messiaen, L., CALLENS, T., ROUX, K., Mortier, G., De Paepe, A., ABRAMOWICZ, M., PERICAK-VANCE, M., et al. (1999). Exon 10b of the NF1 gene represents a mutational hotspot and harbors a recurrent missense mutation Y489C associated with aberrant splicing. GENETICS IN MEDICINE, 1(6), 248–253.
Vancouver
1.
Messiaen L, CALLENS T, ROUX K, Mortier G, De Paepe A, ABRAMOWICZ M, et al. Exon 10b of the NF1 gene represents a mutational hotspot and harbors a recurrent missense mutation Y489C associated with aberrant splicing. GENETICS IN MEDICINE. 1999;1(6):248–53.
MLA
Messiaen, Ludwine, T CALLENS, KJ ROUX, et al. “Exon 10b of the NF1 Gene Represents a Mutational Hotspot and Harbors a Recurrent Missense Mutation Y489C Associated with Aberrant Splicing.” GENETICS IN MEDICINE 1.6 (1999): 248–253. Print.