A novel mitochondrial tRNA Arg mutation resulting in an anticodon swap in a patient with mitochondrial encephalomyopathy. [electronic resource]
Producer: 20131017Description: 571-3 p. digitalISSN:- 1476-5438
- Adolescent
- Anticodon -- genetics
- Base Pairing
- Base Sequence
- Cell Respiration -- physiology
- Cytochrome-c Oxidase Deficiency -- genetics
- Histological Techniques
- Humans
- Male
- Mitochondrial Encephalomyopathies -- genetics
- Molecular Sequence Data
- Muscle, Skeletal -- pathology
- Mutation -- genetics
- Phenotype
- Polymerase Chain Reaction
- Polymorphism, Restriction Fragment Length
- RNA, Transfer, Arg -- genetics
- Sequence Analysis, DNA
- Sweden
No physical items for this record
Publication Type: Case Reports; 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.