A variety of neurologic phenotypes have been described in patients with mitochondrial disorders. We report a 32-year-old man in whom dystonia was the salient and presenting feature of a mitochondrial DNA mutation. He presented at age 23 with writer's cramp and progressed over 5 years to exhibit dyst
โฆ LIBER โฆ
The epidemiology of pathogenic mitochondrial DNA mutations
โ Scribed by P. F. Chinnery; M. A. Johnson; T. M. Wardell; R. Singh-Kler; C. Hayes; D. T. Brown; R. W. Taylor; L. A. Bindoff; D. M. Turnbull
- Publisher
- John Wiley and Sons
- Year
- 2000
- Tongue
- English
- Weight
- 115 KB
- Volume
- 48
- Category
- Article
- ISSN
- 0364-5134
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