Detection of extremely low levels of wild-type mitochondrial DNA in the liver of a patient with Pearson syndrome by a sensitive PCR assay

J Inherit Metab Dis. 1992;15(3):307-10. doi: 10.1007/BF02435963.
No abstract available

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anemia, Sideroblastic / complications
  • Anemia, Sideroblastic / genetics*
  • Base Sequence
  • Bone Marrow Diseases / complications
  • Bone Marrow Diseases / genetics*
  • Bone Marrow Diseases / pathology
  • DNA, Mitochondrial / analysis*
  • Female
  • Humans
  • Infant
  • Liver / chemistry*
  • Molecular Sequence Data
  • Pancreatic Diseases / complications
  • Pancreatic Diseases / genetics*
  • Polymerase Chain Reaction*
  • Syndrome
  • Vacuoles / pathology

Substances

  • DNA, Mitochondrial