Widespread multi-tissue deletions of the mitochondrial genome in the Pearson marrow-pancreas syndrome

J Pediatr. 1990 Oct;117(4):599-602. doi: 10.1016/s0022-3476(05)80698-5.
No abstract available

Publication types

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

MeSH terms

  • Anemia, Sideroblastic / complications
  • Anemia, Sideroblastic / genetics*
  • Anemia, Sideroblastic / pathology
  • Base Sequence
  • Child, Preschool
  • Chromosome Deletion
  • DNA, Mitochondrial / genetics
  • Exocrine Pancreatic Insufficiency / complications
  • Exocrine Pancreatic Insufficiency / genetics*
  • Female
  • Genome, Human*
  • Humans
  • Molecular Sequence Data
  • Stem Cells / ultrastructure
  • Syndrome
  • Vacuoles / ultrastructure

Substances

  • DNA, Mitochondrial