Mitochondrial DNA and disease
- 1 July 1999
- journal article
- review article
- Published by Elsevier in The Lancet
- Vol. 354, S17-S21
- https://doi.org/10.1016/s0140-6736(99)90244-1
Abstract
No abstract availableKeywords
This publication has 29 references indexed in Scilit:
- Genetic Counseling and Prenatal Diagnosis for mtDNA DiseaseAmerican Journal of Human Genetics, 1998
- Epidemiology of A3243G, the Mutation for Mitochondrial Encephalomyopathy, Lactic Acidosis, and Strokelike Episodes: Prevalence of the Mutation in an Adult PopulationAmerican Journal of Human Genetics, 1998
- Familial Progressive Sensorineural Deafness Is Mainly Due to the mtDNA A1555G Mutation and Is Enhanced by Treatment with AminoglycosidesAmerican Journal of Human Genetics, 1998
- Reversal of a mitochondrial DNA defect in human skeletal muscleNature Genetics, 1997
- Selective inhibition of mutant human mitochondrial DNA replication in vitro by peptide nucleic acidsNature Genetics, 1997
- Maternal inheritance and the evaluation of oxidative phosphorylation diseasesThe Lancet, 1996
- A novel heteroplasmic tRNAleu(CUN) mtDNA point mutation in a sporadic patient with mitochondrial encephalomyopathy segregates rapidly in skeletal muscle and suggests an approach to therapyHuman Molecular Genetics, 1996
- MOLECULAR GENETIC ASPECTS OF HUMAN MITOCHONDRIAL DISORDERSAnnual Review of Genetics, 1995
- Mitochondrial DNA Deletions in Progressive External Ophthalmoplegia and Kearns-Sayre SyndromeNew England Journal of Medicine, 1989
- Sequence and organization of the human mitochondrial genomeNature, 1981