Diagnosis of Mitochondrial Disease: Assessment of Mitochondrial DNA Heteroplasmy in Blood
- 1 October 1998
- journal article
- case report
- Published by Elsevier in Biochemical and Biophysical Research Communications
- Vol. 251 (3) , 883-887
- https://doi.org/10.1006/bbrc.1998.9553
Abstract
No abstract availableKeywords
This publication has 20 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
- Clinical features, investigation, and management of patients with defects of mitochondrial DNAJournal of Neurology, Neurosurgery & Psychiatry, 1997
- Mammalian mitochondrial genetics: heredity, heteroplasmy and diseaseTrends in Genetics, 1997
- Molecular pathology of MELAS and MERRF. The relationship between mutation load and clinical phenotypesBrain, 1997
- Recurrent strokes in a 34-year-old manThe Lancet, 1997
- Intracellular Mitochondrial Triplasmy in a Patient with Two Heteroplasmic Base ChangesAmerican Journal of Human Genetics, 1997
- RETRACTED: Mutations in mitochondrial cytochrome c oxidase genes segregate with late-onset Alzheimer diseaseProceedings of the National Academy of Sciences, 1997
- Mitochondrial EncephalomyopathiesArchives of Neurology, 1993
- Presence of mitochondrial-DNA-like sequences in the human nuclear DNAGene, 1983