Broad Phenotypic Heterogeneity and Multisystem Involvement in Single mtDNA Deletion-associated Pearson Syndrome

Lignende værker

• Mitochondrial Ophthalmoplegia Is Not Only due to mtDNA Deletions
  af: Finsterer, Josef
  Udgivet: (2019)
• Comprehensive clinical and genetic work-up of patients carrying single mtDNA deletions is warranted
  af: Finsterer, Josef
  Udgivet: (2021)
• mtDNA Deletion in an Iranian Infant with Pearson Marrow Syndrome
  af: Arzanian, Mohammad Taghi, et al.
  Udgivet: (2010)
• Phenotypic spectrum of FARS2-deficiency
  af: Finsterer, Josef, et al.
  Udgivet: (2017)
• Pearson syndrome and mitochondrial encephalomyopathy in a patient with a deletion of mtDNA.
  af: McShane, M A, et al.
  Udgivet: (1991)