Recessive POLG mutations presenting with sensory and ataxic neuropathy in compound heterozygote patients with progressive external ophthalmoplegia
(2003) NEUROMUSCULAR DISORDERS. 13(2). p.133-142
Please use this url to cite or link to this publication:
http://hdl.handle.net/1854/LU-3200814
- author
- G Van Goethem, JJ Martin, Bart Dermaut UGent, A Löfgren, A Wibail, D Ververken, P Tack, I Dehaene, M Van Zandijcke, M Moonen, C Ceuterick, P De Jonghe and C Van Broeckhoven
- organization
- year
- 2003
- 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.