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Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE)-like phenotype in a patient with a novel heterozygous POLG mutation.

Publication ,  Journal Article
Prasun, P; Koeberl, DD
Published in: J Neurol
September 2014

Duke Scholars

Published In

J Neurol

DOI

EISSN

1432-1459

Publication Date

September 2014

Volume

261

Issue

9

Start / End Page

1818 / 1819

Location

Germany

Related Subject Headings

  • Phenotype
  • Neurology & Neurosurgery
  • Mutation
  • Mitochondrial Encephalomyopathies
  • Male
  • Magnetic Resonance Imaging
  • Humans
  • Heterozygote
  • DNA-Directed DNA Polymerase
  • DNA Polymerase gamma
 

Citation

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Prasun, P., & Koeberl, D. D. (2014). Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE)-like phenotype in a patient with a novel heterozygous POLG mutation. J Neurol, 261(9), 1818–1819. https://doi.org/10.1007/s00415-014-7428-2
Prasun, Pankaj, and Dwight D. Koeberl. “Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE)-like phenotype in a patient with a novel heterozygous POLG mutation.J Neurol 261, no. 9 (September 2014): 1818–19. https://doi.org/10.1007/s00415-014-7428-2.
Prasun, Pankaj, and Dwight D. Koeberl. “Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE)-like phenotype in a patient with a novel heterozygous POLG mutation.J Neurol, vol. 261, no. 9, Sept. 2014, pp. 1818–19. Pubmed, doi:10.1007/s00415-014-7428-2.
Journal cover image

Published In

J Neurol

DOI

EISSN

1432-1459

Publication Date

September 2014

Volume

261

Issue

9

Start / End Page

1818 / 1819

Location

Germany

Related Subject Headings

  • Phenotype
  • Neurology & Neurosurgery
  • Mutation
  • Mitochondrial Encephalomyopathies
  • Male
  • Magnetic Resonance Imaging
  • Humans
  • Heterozygote
  • DNA-Directed DNA Polymerase
  • DNA Polymerase gamma