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.

Authors

D D de Vries¹, W Ruitenbeek, B A van Oost

Affiliation

¹ Department of Human Genetics, University Hospital Nijmegen, The Netherlands.

PMID: 1405463
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