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Exhaustive mutation analysis of the NF1 gene allows identification of 95% of mutations and reveals a high frequency of unusual splicing defects.

Ludwine Messiaen, T CALLENS, Geert Mortier, DIANE BEYSEN, Ina Vandenbroucke, Nadine Van Roy UGent, Franki Speleman UGent and Anne De Paepe UGent (2000) HUMAN MUTATION. 15(6). p.541-555
Please use this url to cite or link to this publication:
author
organization
year
type
journalArticle (original)
publication status
published
subject
journal title
HUMAN MUTATION
Hum. Mutat.
volume
15
issue
6
pages
541-555 pages
Web of Science type
Article
Web of Science id
000087455300006
ISSN
1059-7794
language
English
UGent publication?
yes
classification
A1
id
126953
handle
http://hdl.handle.net/1854/LU-126953
date created
2004-01-14 13:36:00
date last changed
2016-12-19 15:38:53
@article{126953,
  author       = {Messiaen, Ludwine and CALLENS, T and Mortier, Geert and BEYSEN, DIANE and Vandenbroucke, Ina and Van Roy, Nadine and Speleman, Franki and De Paepe, Anne},
  issn         = {1059-7794},
  journal      = {HUMAN MUTATION},
  language     = {eng},
  number       = {6},
  pages        = {541--555},
  title        = {Exhaustive mutation analysis of the NF1 gene allows identification of 95\% of mutations and reveals a high frequency of unusual splicing defects.},
  volume       = {15},
  year         = {2000},
}

Chicago
Messiaen, Ludwine, T CALLENS, Geert Mortier, Diane Beysen, Ina Vandenbroucke, Nadine Van Roy, Franki Speleman, and Anne De Paepe. 2000. “Exhaustive Mutation Analysis of the NF1 Gene Allows Identification of 95% of Mutations and Reveals a High Frequency of Unusual Splicing Defects.” Human Mutation 15 (6): 541–555.
APA
Messiaen, L., CALLENS, T., Mortier, G., Beysen, D., Vandenbroucke, I., Van Roy, N., Speleman, F., et al. (2000). Exhaustive mutation analysis of the NF1 gene allows identification of 95% of mutations and reveals a high frequency of unusual splicing defects. HUMAN MUTATION, 15(6), 541–555.
Vancouver
1.
Messiaen L, CALLENS T, Mortier G, Beysen D, Vandenbroucke I, Van Roy N, et al. Exhaustive mutation analysis of the NF1 gene allows identification of 95% of mutations and reveals a high frequency of unusual splicing defects. HUMAN MUTATION. 2000;15(6):541–55.
MLA
Messiaen, Ludwine, T CALLENS, Geert Mortier, et al. “Exhaustive Mutation Analysis of the NF1 Gene Allows Identification of 95% of Mutations and Reveals a High Frequency of Unusual Splicing Defects.” HUMAN MUTATION 15.6 (2000): 541–555. Print.