Detection of extremely low levels of wild‐type mitochondrial DNA in the liver of a patient with pearson syndrome by a sensitive PCR assay
- 1 May 1992
- journal article
- Published by Wiley in Journal of Inherited Metabolic Disease
- Vol. 15 (3) , 307-310
- https://doi.org/10.1007/bf02435963
Abstract
No abstract availableThis publication has 10 references indexed in Scilit:
- Site-specific deletions of the mitochondrial genome in the Pearson marrow-pancreas syndromeGenomics, 1991
- Pearson's marrow-pancreas syndrome. A multisystem mitochondrial disorder in infancy.Journal of Clinical Investigation, 1990
- Widespread multitissue deletions of the mitochondrial genome in the Pearson marrow-pancreas syndromePublished by Elsevier ,1990
- Mitochondrial myopathies: Clinical and biochemical features of 30 patients with major deletions of muscle mitochondrial DNAAnnals of Neurology, 1989
- Mitochondrial DNA Deletions in Progressive External Ophthalmoplegia and Kearns-Sayre SyndromeNew England Journal of Medicine, 1989
- MITOCHONDRIAL DNA DELETION IN PEARSON'S MARROW/PANCREAS SYNDROMEPublished by Elsevier ,1989
- KEARNS-SAYRE SYNDROME WITH MUSCLE MITOCHONDRIAL DNA DELETIONThe Lancet, 1988
- Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathiesNature, 1988
- Sequence and organization of the human mitochondrial genomeNature, 1981
- A new syndrome of refractory sideroblastic anemia with vacuolization of marrow precursors and exocrine pancreatic dysfunctionPublished by Elsevier ,1979