Article
Mitochondrial disorders.
The Japanese journal of human genetics - 1 Dec 1997
DiMauro S, Tanji K
Abstract excerpt
In this minireview, we attempt to survey the three main group of mitochondrial disorders, defects of nuclear DNA, defects of mitochondrial DNA, and defects of intergenomic signaling, with emphasis on recent contributions and pathogenetic mechanisms. In so doing, we have tried to point out some of...
Topics
- Central Nervous System Diseases
- DNA, Mitochondrial
- Gene Deletion
- Genotype
- Humans
- Mitochondrial Encephalomyopathies
- Mutation
- Phenotype