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Digenic progressive external ophthalmoplegiain a sporadic patient: recessive mutationsin POLG and C10orf2/Twinkle

Gert Van Goethem, Ann Löfgren, Bart Dermaut UGent, Chantal Ceuterick, Jean-Jacques Martin and Christine Van Broeckhoven (2003) HUMAN MUTATION. 22(2). p.175-176
Please use this url to cite or link to this publication:
author
organization
year
type
journalArticle (letterNote)
publication status
published
subject
keyword
MNGIE, TWINKLE, GENE, ENCEPHALOMYOPATHY, FEATURES, DISORDER, MULTIPLE MTDNA DELETIONS, MITOCHONDRIAL-DNA DELETIONS
journal title
HUMAN MUTATION
Hum. Mutat.
volume
22
issue
2
pages
175 - 176
Web of Science type
Letter
Web of Science id
000184532800011
JCR category
GENETICS & HEREDITY
JCR impact factor
6.328 (2003)
JCR rank
14/115 (2003)
JCR quartile
1 (2003)
ISSN
1059-7794
DOI
10.1002/humu.10246
language
English
UGent publication?
no
classification
A1
copyright statement
I have transferred the copyright for this publication to the publisher
id
3200775
handle
http://hdl.handle.net/1854/LU-3200775
date created
2013-04-24 15:08:59
date last changed
2016-12-19 15:43:12
@article{3200775,
  author       = {Van Goethem, Gert and L{\"o}fgren, Ann and Dermaut, Bart and Ceuterick, Chantal and Martin, Jean-Jacques and Van Broeckhoven, Christine},
  issn         = {1059-7794},
  journal      = {HUMAN MUTATION},
  keyword      = {MNGIE,TWINKLE,GENE,ENCEPHALOMYOPATHY,FEATURES,DISORDER,MULTIPLE MTDNA DELETIONS,MITOCHONDRIAL-DNA DELETIONS},
  language     = {eng},
  number       = {2},
  pages        = {175--176},
  title        = {Digenic progressive external ophthalmoplegiain a sporadic patient: recessive mutationsin POLG and C10orf2/Twinkle},
  url          = {http://dx.doi.org/10.1002/humu.10246},
  volume       = {22},
  year         = {2003},
}

Chicago
Van Goethem, Gert, Ann Löfgren, Bart Dermaut, Chantal Ceuterick, Jean-Jacques Martin, and Christine Van Broeckhoven. 2003. “Digenic Progressive External Ophthalmoplegiain a Sporadic Patient: Recessive Mutationsin POLG and C10orf2/Twinkle.” Human Mutation 22 (2): 175–176.
APA
Van Goethem, Gert, Löfgren, A., Dermaut, B., Ceuterick, C., Martin, J.-J., & Van Broeckhoven, C. (2003). Digenic progressive external ophthalmoplegiain a sporadic patient: recessive mutationsin POLG and C10orf2/Twinkle. HUMAN MUTATION, 22(2), 175–176.
Vancouver
1.
Van Goethem G, Löfgren A, Dermaut B, Ceuterick C, Martin J-J, Van Broeckhoven C. Digenic progressive external ophthalmoplegiain a sporadic patient: recessive mutationsin POLG and C10orf2/Twinkle. HUMAN MUTATION. 2003;22(2):175–6.
MLA
Van Goethem, Gert, Ann Löfgren, Bart Dermaut, et al. “Digenic Progressive External Ophthalmoplegiain a Sporadic Patient: Recessive Mutationsin POLG and C10orf2/Twinkle.” HUMAN MUTATION 22.2 (2003): 175–176. Print.