Site-specific deletions of the mitochondrial genome in the Pearson marrow-pancreas syndrome
- 30 June 1991
- Vol. 10 (2) , 502-504
- https://doi.org/10.1016/0888-7543(91)90342-c
Abstract
No abstract availableKeywords
This publication has 10 references indexed in Scilit:
- Pearson's marrow-pancreas syndrome. A multisystem mitochondrial disorder in infancy.Journal of Clinical Investigation, 1990
- Characterization of human MRP/Th RNA and its nuclear gene: full length MRP/Th RNA is an active endoribonuclease when assembled as an RNPNucleic Acids Research, 1990
- Recombination via flanking direct repeats is a major cause of large-scale deletions of human mitochondrial DNANucleic Acids Research, 1990
- An autosomal dominant disorder with multiple deletions of mitochondrial DNA starting at the D-loop regionNature, 1989
- MITOCHONDRIAL DNA DELETION IN PEARSON'S MARROW/PANCREAS SYNDROMEPublished by Elsevier ,1989
- A Direct Repeat Is a Hotspot for Large-Scale Deletion of Human Mitochondrial DNAScience, 1989
- Deletions of muscle mitochondrial DNA in mitochondrial myopathies: sequence analysis and possible mechanismsNucleic Acids Research, 1989
- Copy choice illegitimate DNA recombinationCell, 1988
- The tRNA genes punctuate the reading of genetic information in human mitochondrial DNACell, 1980
- A new syndrome of refractory sideroblastic anemia with vacuolization of marrow precursors and exocrine pancreatic dysfunctionPublished by Elsevier ,1979