Melas associated with mutations in the polg1 gene

Neurology. 2008 Mar 25;70(13):1054; author reply 1054-5. doi: 10.1212/01.wnl.0000307661.98694.c3.
No abstract available

Publication types

  • Case Reports
  • Letter
  • Comment

MeSH terms

  • Adolescent
  • Adult
  • Brain Infarction / classification
  • Brain Infarction / diagnosis*
  • Brain Infarction / genetics
  • DNA Polymerase gamma
  • DNA, Mitochondrial / genetics
  • DNA-Directed DNA Polymerase / genetics*
  • Diagnosis, Differential
  • Diagnostic Errors / prevention & control
  • Genetic Markers / genetics
  • Humans
  • MELAS Syndrome / diagnosis*
  • MELAS Syndrome / genetics
  • MELAS Syndrome / physiopathology
  • Mitochondrial Diseases / diagnosis
  • Mitochondrial Diseases / genetics
  • Mitochondrial Diseases / physiopathology
  • Mutation / genetics*
  • Occipital Lobe / blood supply
  • Occipital Lobe / pathology
  • Occipital Lobe / physiopathology

Substances

  • DNA, Mitochondrial
  • Genetic Markers
  • DNA Polymerase gamma
  • DNA-Directed DNA Polymerase
  • POLG protein, human