Comprehensive clinical and genetic work-up of patients carrying single mtDNA deletions is warranted

Benzer Materyaller

• Mitochondrial Ophthalmoplegia Is Not Only due to mtDNA Deletions
  Yazar:: Finsterer, Josef
  Baskı/Yayın Bilgisi: (2019)
• Broad Phenotypic Heterogeneity and Multisystem Involvement in Single mtDNA Deletion-associated Pearson Syndrome
  Yazar:: Finsterer, Josef, ve diğerleri
  Baskı/Yayın Bilgisi: (2018)
• Unmasking fibromyalgia as a mitochondrial disorder requires search for more than a single variant or single mtDNA deletions
  Yazar:: Finsterer, Josef
  Baskı/Yayın Bilgisi: (2020)
• Comprehensive work-up is warranted for patients with severe COVID-19 and muscle weakness including respiratory muscles
  Yazar:: Finsterer, Josef
  Baskı/Yayın Bilgisi: (2021)
• Comment on “CPEO and Mitochondrial Myopathy in a Patient with DGUOK Compound Heterozygous Pathogenetic Variant and mtDNA Multiple Deletions”
  Yazar:: Finsterer, Josef
  Baskı/Yayın Bilgisi: (2020)