Mitochondrial DNA mutations in Leigh syndrome and their phylogenetic implications. [electronic resource]
Producer: 20000414Description: 69-75 p. digitalISSN:- 1434-5161
- Adenosine Triphosphatases -- genetics
- Age of Onset
- Child
- Child, Preschool
- DNA Mutational Analysis
- DNA, Mitochondrial -- genetics
- Electron Transport Complex IV -- genetics
- Female
- Humans
- Infant
- Leigh Disease -- enzymology
- Male
- Microscopy, Electron
- Muscle, Skeletal -- pathology
- Phylogeny
- Point Mutation
- Polymerase Chain Reaction
- Polymorphism, Restriction Fragment Length
- Pyruvate Dehydrogenase Complex -- genetics
No physical items for this record
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
There are no comments on this title.
Log in to your account to post a comment.