Axonal neuropathy with optic atrophy is caused by mutations in mitofusin 2. [electronic resource]
Producer: 20060425Description: 276-81 p. digitalISSN:- 0364-5134
- Adolescent
- Adult
- Age of Onset
- Charcot-Marie-Tooth Disease -- complications
- Child
- DNA Mutational Analysis -- methods
- Family Health
- GTP Phosphohydrolases
- Genetic Predisposition to Disease -- genetics
- Humans
- Membrane Proteins -- genetics
- Middle Aged
- Mitochondrial Proteins -- genetics
- Models, Biological
- Mutation
- Neural Conduction -- physiology
- Optic Atrophy -- etiology
- Pedigree
- Visual Acuity -- physiology
No physical items for this record
Publication Type: Comparative Study; Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
There are no comments on this title.
Log in to your account to post a comment.