Coamplification of Nuclear Pseudogenes and Assessment of Heteroplasmy of Mitochondrial DNA Mutations
- 1 June 1998
- journal article
- Published by Elsevier in Biochemical and Biophysical Research Communications
- Vol. 247 (1) , 57-59
- https://doi.org/10.1006/bbrc.1998.8666
Abstract
No abstract availableKeywords
This publication has 8 references indexed in Scilit:
- Ancient mtDNA sequences in the human nuclear genome: A potential source of errors in identifying pathogenic mutationsProceedings of the National Academy of Sciences, 1997
- Apparent mtDNA heteroplasmy in Alzheimer’s disease patients and in normals due to PCR amplification of nucleus-embedded mtDNA pseudogenesProceedings of the National Academy of Sciences, 1997
- Biochemical and molecular investigations in respiratory chain deficienciesClinica Chimica Acta; International Journal of Clinical Chemistry, 1994
- DISEASES OF THE MITOCHONDRIAL DNAAnnual Review of Biochemistry, 1992
- Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke‐like episodes (MELAS)Neurology, 1992
- Pearson's marrow-pancreas syndrome. A multisystem mitochondrial disorder in infancy.Journal of Clinical Investigation, 1990
- Human Cells Lacking mtDNA: Repopulation with Exogenous Mitochondria by ComplementationScience, 1989
- Presence of mitochondrial-DNA-like sequences in the human nuclear DNAGene, 1983