MELAS syndrome due to the m.3291T > C mutation

Podobne knjige/članki

• Onset of MELAS due to the m.3243A > G mutation is early if the large phenotypic variability is considered()()
  od: Finsterer, Josef, et al.
  Izdano: (2016)
• Arrhythmias in MELAS syndrome
  od: Finsterer, Josef, et al.
  Izdano: (2016)
• Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-like Episodes (MELAS) due to a m.10158T>C ND3 Mutation with a Normal Muscle Biopsy
  od: Finsterer, Josef, et al.
  Izdano: (2017)
• Arrhythmias in MELAS syndrome
  od: Josef Finsterer, et al.
  Izdano: (2016-06-01)
• Mitochondrial vasculopathy due to the m.3243A > G mutation is not restricted to the carotid artery
  od: Finsterer, Josef, et al.
  Izdano: (2016)