Annotation: Mitochondrial genotype and clinical phenotype
- 1 June 1998
- journal article
- review article
- Published by Wiley in Journal of Inherited Metabolic Disease
- Vol. 21 (4) , 321-325
- https://doi.org/10.1023/a:1005357221101
Abstract
No abstract availableThis publication has 29 references indexed in Scilit:
- Tissue-specific selection for different mtDNA genotypes in heteroplasmic miceNature Genetics, 1997
- Mitochondrial encephalomyopathies: gene mutationNeuromuscular Disorders, 1997
- Maternal inheritance and the evaluation of oxidative phosphorylation diseasesThe Lancet, 1996
- Mitochondrial DNA and RNA processing in MELASAnnals of Neurology, 1996
- Mitochondrial diabetes mellitus: a reviewBiochimica et Biophysica Acta (BBA) - Molecular Basis of Disease, 1995
- MtDNA mutation in MERRF syndrome causes defective aminoacylation of tRNALys and premature translation terminationNature Genetics, 1995
- Extremely high levels of mutant mtDNAs co-localize with cytocohrome c oxidase-negative ragged-red fibers in patients harboring a point mutation at nt 3243Human Molecular Genetics, 1994
- Atypical clinical presentations associated with the MELAS mutation at position 3243 of human mitochondrial DNANeuromuscular Disorders, 1993
- MELAS: Clinical features, biochemistry, and molecular geneticsAnnals of Neurology, 1992
- Mitochondrial DNA Mutation Associated with Leber's Hereditary Optic NeuropathyScience, 1988