Preferential amplification and molecular characterization of junction sequences of a pathogenetic deletion in human mitochondrial DNA
- 29 October 1989
- Vol. 5 (3) , 623-628
- https://doi.org/10.1016/0888-7543(89)90032-3
Abstract
No abstract availableThis publication has 22 references indexed in Scilit:
- DELETIONS OF MUSCLE MITOCHONDRIAL DNAThe Lancet, 1988
- DNA typing from single hairsNature, 1988
- KEARNS-SAYRE SYNDROME WITH MUSCLE MITOCHONDRIAL DNA DELETIONThe Lancet, 1988
- Injection of mitochondria into human cells leads to a rapid replacement of the endogenous mitochondrial DNACell, 1988
- Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathiesNature, 1988
- Mitochondrial Inheritance in a Mitochondrially Mediated DiseaseNew England Journal of Medicine, 1983
- Sequence and organization of the human mitochondrial genomeNature, 1981
- TRANSMISSION GENETICS OF MITOCHONDRIA AND CHLOROPLASTSAnnual Review of Genetics, 1978
- Lumping or splitting? “ophthalmoplegia‐plus” or kearns‐sayre syndrome?Annals of Neurology, 1977
- The Number of Mitochondrial Deoxyribonucleic Acid Genomes in Mouse L and Human HeLa CellsJournal of Biological Chemistry, 1974