Mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes with an mt-tl1 m.3243a>g point mutation: neuroradiological features and their implications for underlying pathogenesis

HIGHLIGHTS

• who: Helin Zheng from the Azienda USL Toscana Nord Ovest, Italy Mediterranea University of Reggio have published the research: Mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes with an MT-TL1 m.3243A>G point mutation: Neuroradiological features and their implications for underlying pathogenesis, in the Journal: (JOURNAL)
• what: The authors propose the concept of lesion polymorphism.
• how: The clinical data and genetic results were obtained from patients` medical records and imaging data were analyzed and recorded based on the imaging records. In the study the supplying vessel of the lesion was . . .
  

   

  

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