## Abstract Mutations in the dysferlin gene cause limbβgirdle muscular dystrophy type 2B (LGMD2B). The involvement of the central nervous system in dysferlinopathy has not been described. We describe the clinical features of a patient with LGMD2B associated with dysferlin mutations (homozygous G337
β¦ LIBER β¦
Hyperthyroidism as a cause of persistent choreic movements
β Scribed by P. J. Delwaide; J. Schoenen
- Book ID
- 114780764
- Publisher
- John Wiley and Sons
- Year
- 2009
- Tongue
- English
- Weight
- 245 KB
- Volume
- 58
- Category
- Article
- ISSN
- 0001-6314
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