Extended spinal cord involvement in adult-onset Leigh syndrome due to mitochondrial 10197G A mutation
- Resource Type
- Source
- Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology. 43(12)
- Subject
Adult Optic Atrophies, Hereditary Spinal Cord Mutation Humans Leigh Disease DNA, Mitochondrial - Language
- ISSN
- 1590-3478