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Recessive POLG mutations presenting with sensory and ataxic neuropathy in compound heterozygote patients with progressive external ophthalmoplegia

G Van Goethem, JJ Martin, Bart Dermaut UGent, A Löfgren, A Wibail, D Ververken, P Tack, I Dehaene, M Van Zandijcke, M Moonen, et al. (2003) NEUROMUSCULAR DISORDERS. 13(2). p.133-142
Please use this url to cite or link to this publication:
author
organization
year
type
journalArticle (original)
publication status
published
subject
keyword
sensory and ataxic neuropathy, mitochondrial DNA polymerase gamma, multiple mitochondrial DNA deletions, MITOCHONDRIAL-DNA DELETIONS, MULTIPLE MTDNA DELETIONS, KEARNS-SAYRE SYNDROME, AUTOSOMAL-DOMINANT, GENETIC FEATURES, POLYMERASE-GAMMA, DISORDER, MYOPATHY, DISEASE, FAMILY, progressive external ophthalmoplegia, autosomal recessive inheritance
journal title
NEUROMUSCULAR DISORDERS
Neuromusc. Disord.
volume
13
issue
2
pages
133 - 142
Web of Science type
Article
Web of Science id
000181136000003
JCR category
NEUROSCIENCES
JCR impact factor
2.894 (2003)
JCR rank
62/197 (2003)
JCR quartile
2 (2003)
ISSN
0960-8966
DOI
10.1016/S0960-8966(02)00216-X
language
English
UGent publication?
no
classification
A1
copyright statement
I have transferred the copyright for this publication to the publisher
id
3200814
handle
http://hdl.handle.net/1854/LU-3200814
date created
2013-04-24 15:08:59
date last changed
2016-12-19 15:43:12
@article{3200814,
  author       = {Van Goethem, G and Martin, JJ and Dermaut, Bart and L{\"o}fgren, A and Wibail, A and Ververken, D and Tack, P and Dehaene, I and Van Zandijcke, M and Moonen, M and Ceuterick, C and De Jonghe, P and Van Broeckhoven, C},
  issn         = {0960-8966},
  journal      = {NEUROMUSCULAR DISORDERS},
  keyword      = {sensory and ataxic neuropathy,mitochondrial DNA polymerase gamma,multiple mitochondrial DNA deletions,MITOCHONDRIAL-DNA DELETIONS,MULTIPLE MTDNA DELETIONS,KEARNS-SAYRE SYNDROME,AUTOSOMAL-DOMINANT,GENETIC FEATURES,POLYMERASE-GAMMA,DISORDER,MYOPATHY,DISEASE,FAMILY,progressive external ophthalmoplegia,autosomal recessive inheritance},
  language     = {eng},
  number       = {2},
  pages        = {133--142},
  title        = {Recessive POLG mutations presenting with sensory and ataxic neuropathy in compound heterozygote patients with progressive external ophthalmoplegia},
  url          = {http://dx.doi.org/10.1016/S0960-8966(02)00216-X},
  volume       = {13},
  year         = {2003},
}

Chicago
Van Goethem, G, JJ Martin, Bart Dermaut, A Löfgren, A Wibail, D Ververken, P Tack, et al. 2003. “Recessive POLG Mutations Presenting with Sensory and Ataxic Neuropathy in Compound Heterozygote Patients with Progressive External Ophthalmoplegia.” Neuromuscular Disorders 13 (2): 133–142.
APA
Van Goethem, G, Martin, J., Dermaut, B., Löfgren, A., Wibail, A., Ververken, D., Tack, P., et al. (2003). Recessive POLG mutations presenting with sensory and ataxic neuropathy in compound heterozygote patients with progressive external ophthalmoplegia. NEUROMUSCULAR DISORDERS, 13(2), 133–142.
Vancouver
1.
Van Goethem G, Martin J, Dermaut B, Löfgren A, Wibail A, Ververken D, et al. Recessive POLG mutations presenting with sensory and ataxic neuropathy in compound heterozygote patients with progressive external ophthalmoplegia. NEUROMUSCULAR DISORDERS. 2003;13(2):133–42.
MLA
Van Goethem, G, JJ Martin, Bart Dermaut, et al. “Recessive POLG Mutations Presenting with Sensory and Ataxic Neuropathy in Compound Heterozygote Patients with Progressive External Ophthalmoplegia.” NEUROMUSCULAR DISORDERS 13.2 (2003): 133–142. Print.