Identification of point mutations by mispairing PCR as exemplified in MERRF disease
- 1 December 1990
- journal article
- research article
- Published by Elsevier in Biochemical and Biophysical Research Communications
- Vol. 173 (2) , 561-565
- https://doi.org/10.1016/s0006-291x(05)80071-3
Abstract
No abstract availableThis publication has 5 references indexed in Scilit:
- 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
- Familial mitochondrial encephalomyopathy (MERRF): Genetic, pathophysiological, and biochemical characterization of a mitochondrial DNA diseaseCell, 1988
- DNA typing from single hairsNature, 1988
- Sequence and organization of the human mitochondrial genomeNature, 1981