Leber's hereditary optic neuropathy associated with a disorder indistinguishable from multiple sclerosis in a male harbouring the mitochondrial DNA 11778 mutation. [electronic resource]
Producer: 19950911Description: 326-9 p. digitalISSN:- 0001-6314
- Adult
- Base Composition -- genetics
- Brain -- pathology
- DNA Mutational Analysis
- DNA, Mitochondrial -- genetics
- Electroencephalography
- Gene Frequency
- Humans
- Immunoglobulins -- cerebrospinal fluid
- Magnetic Resonance Imaging
- Male
- Multiple Sclerosis -- diagnosis
- Neurologic Examination
- Oligoclonal Bands
- Optic Atrophies, Hereditary -- diagnosis
- Optic Nerve -- pathology
- Pedigree
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.