OPA1 mutations in Japanese patients suspected to have autosomal dominant optic atrophy. [electronic resource]
Producer: 20120509Description: 91-7 p. digitalISSN:- 1613-2246
- Adolescent
- Adult
- Asian People -- genetics
- DNA Mutational Analysis
- DNA, Mitochondrial -- genetics
- Female
- GTP Phosphohydrolases -- genetics
- Humans
- Japan
- Male
- Middle Aged
- Mutation
- Optic Atrophy, Autosomal Dominant -- genetics
- Pedigree
- Polymerase Chain Reaction
- Visual Acuity -- physiology
- Visual Fields -- physiology
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.