Mutations in the ND5 subunit of complex I of the mitochondrial DNA are a frequent cause of oxidative phosphorylation disease. [electronic resource]
Producer: 20070514Description: e74 p. digitalISSN:- 1468-6244
- Amino Acid Sequence
- Animals
- Brain -- abnormalities
- Child
- Chromatography, High Pressure Liquid
- DNA Mutational Analysis
- DNA, Mitochondrial -- genetics
- Diseases in Twins
- Electron Transport Complex I -- chemistry
- Fatal Outcome
- Female
- Genetic Testing
- Humans
- Hydrophobic and Hydrophilic Interactions
- Infant, Newborn
- Leigh Disease -- genetics
- MELAS Syndrome -- genetics
- Male
- Mitochondria, Muscle -- enzymology
- Mitochondrial Diseases -- genetics
- Mitochondrial Proteins -- chemistry
- Molecular Sequence Data
- Mutation, Missense
- Oxidative Phosphorylation
- Phenotype
- Protein Subunits
- Sequence Alignment
- Sequence Homology, Amino Acid
No physical items for this record
Publication Type: Case Reports; Journal Article
There are no comments on this title.
Log in to your account to post a comment.