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A new mitochondrial point mutation in the transfer RNA(Leu) gene in a patient with a clinical phenotype resembling Kearns-Sayre syndrome.

S SENECA, H VERHELST, L DE MEIRLEIR, Françoise Meire UGent, C GROOTE, W LISSENS and Rudy Van Coster UGent (2001) ARCHIVES OF NEUROLOGY. 58(7). p.1113-1118
Please use this url to cite or link to this publication:
author
organization
year
type
journalArticle (original)
publication status
published
subject
journal title
ARCHIVES OF NEUROLOGY
Arch. Neurol.
volume
58
issue
7
pages
1113-1118 pages
Web of Science type
Article
Web of Science id
000169825300010
JCR category
CLINICAL NEUROLOGY
JCR impact factor
4.053 (2001)
JCR rank
10/135 (2001)
JCR quartile
1 (2001)
ISSN
0003-9942
language
English
UGent publication?
yes
classification
A1
id
141141
handle
http://hdl.handle.net/1854/LU-141141
date created
2004-01-14 13:37:00
date last changed
2016-12-19 15:38:32
@article{141141,
  author       = {SENECA, S and VERHELST, H and DE MEIRLEIR, L and Meire, Fran\c{c}oise and GROOTE, C and LISSENS, W and Van Coster, Rudy},
  issn         = {0003-9942},
  journal      = {ARCHIVES OF NEUROLOGY},
  language     = {eng},
  number       = {7},
  pages        = {1113--1118},
  title        = {A new mitochondrial point mutation in the transfer RNA(Leu) gene in a patient with a clinical phenotype resembling Kearns-Sayre syndrome.},
  volume       = {58},
  year         = {2001},
}

Chicago
SENECA, S, H VERHELST, L DE MEIRLEIR, Françoise Meire, C GROOTE, W LISSENS, and Rudy Van Coster. 2001. “A New Mitochondrial Point Mutation in the Transfer RNA(Leu) Gene in a Patient with a Clinical Phenotype Resembling Kearns-Sayre Syndrome.” Archives of Neurology 58 (7): 1113–1118.
APA
SENECA, S., VERHELST, H., DE MEIRLEIR, L., Meire, F., GROOTE, C., LISSENS, W., & Van Coster, R. (2001). A new mitochondrial point mutation in the transfer RNA(Leu) gene in a patient with a clinical phenotype resembling Kearns-Sayre syndrome. ARCHIVES OF NEUROLOGY, 58(7), 1113–1118.
Vancouver
1.
SENECA S, VERHELST H, DE MEIRLEIR L, Meire F, GROOTE C, LISSENS W, et al. A new mitochondrial point mutation in the transfer RNA(Leu) gene in a patient with a clinical phenotype resembling Kearns-Sayre syndrome. ARCHIVES OF NEUROLOGY. 2001;58(7):1113–8.
MLA
SENECA, S, H VERHELST, L DE MEIRLEIR, et al. “A New Mitochondrial Point Mutation in the Transfer RNA(Leu) Gene in a Patient with a Clinical Phenotype Resembling Kearns-Sayre Syndrome.” ARCHIVES OF NEUROLOGY 58.7 (2001): 1113–1118. Print.