Use of single strand conformation polymorphism analysis to detect point mutations in human mitochondrial DNA
- 30 September 1992
- journal article
- Published by Elsevier in Journal of the Neurological Sciences
- Vol. 111 (2), 222-226
- https://doi.org/10.1016/0022-510x(92)90074-u
Abstract
No abstract availableKeywords
This publication has 19 references indexed in Scilit:
- Quantitation of mitochondrial DNA carrying tRNALys mutation in MERRF patientsBiochemical and Biophysical Research Communications, 1991
- Clinical spectrum of mitochondrial DNA mutation at base pair 8344The Lancet, 1991
- Mitochondrial encephalopathies: molecular genetic diagnosis from blood samplesThe Lancet, 1991
- Identification of point mutations by mispairing PCR as exemplified in MERRF diseaseBiochemical and Biophysical Research Communications, 1990
- A major segment of the neurofibromatosis type 1 gene: cDNA sequence, genomic structure, and point mutationsCell, 1990
- Multiple mutations in highly conserved residues are found in mildly affected cystic fibrosis patientsCell, 1990
- Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNALys mutationCell, 1990
- Rapid and sensitive detection of point mutations and DNA polymorphisms using the polymerase chain reactionGenomics, 1989
- Primer-Directed Enzymatic Amplification of DNA with a Thermostable DNA PolymeraseScience, 1988
- Sequence and organization of the human mitochondrial genomeNature, 1981