Mitochondrial myopathy plus due to the variant m.586G > A in MT-TF

Lignende værker

• Expanding the clinical spectrum of MTTF mutations
  af: Barcia, Giulia, et al.
  Udgivet: (2019)
• Cytochrome c oxidase deficiency caused by biallelic SCO2 mutations in two sibs with cerebellar ataxia and progressive peripheral axonal neuropathy
  af: Barcia, Giulia, et al.
  Udgivet: (2019)
• Mitochondrial myopathy plus due to the variant m.586G > A in MT-TF
  af: Finsterer, Josef
  Udgivet: (2019)
• Biallelic IARS2 mutations presenting as sideroblastic anemia
  af: Barcia, Giulia, et al.
  Udgivet: (2021)
• Novel FARS2 variants in patients with early onset encephalopathy with or without epilepsy associated with long survival
  af: Barcia, Giulia, et al.
  Udgivet: (2020)