The mitochondrial genome and mitochondrial muscle disorders
- 14 May 2001
- journal article
- review article
- Published by Elsevier in Current Opinion in Pharmacology
- Vol. 1 (3) , 288-293
- https://doi.org/10.1016/s1471-4892(01)00051-0
Abstract
No abstract availableKeywords
This publication has 57 references indexed in Scilit:
- Generation of mice with mitochondrial dysfunction by introducing mouse mtDNA carrying a deletion into zygotesNature Genetics, 2000
- Peptide nucleic acid delivery to human mitochondriaGene Therapy, 1999
- Aging-Dependent Large Accumulation of Point Mutations in the Human mtDNA Control Region for ReplicationScience, 1999
- Genetic Counseling and Prenatal Diagnosis for mtDNA DiseaseAmerican Journal of Human Genetics, 1998
- Role of mitochondrial DNA mutations in human aging: Implications for the central nervous system and muscleAnnals of Neurology, 1998
- Maternal inheritance and the evaluation of oxidative phosphorylation diseasesThe Lancet, 1996
- Presentation and clinical investigation of mitochondrial respiratory chain disease. A study of 51 patientsBrain, 1995
- Increase of deleted mitochondrial DNA in the striatum in Parkinson's disease and senescenceBiochemical and Biophysical Research Communications, 1990
- Mitochondrial DNA Deletions in Progressive External Ophthalmoplegia and Kearns-Sayre SyndromeNew England Journal of Medicine, 1989
- Mitochondrial DNA Mutation Associated with Leber's Hereditary Optic NeuropathyScience, 1988