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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
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Keywords
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

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Citation

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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.
@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},
}

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