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

פריטים דומים

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