Inflammation and response to steroid treatment in limb-girdle muscular dystrophy 2I
✍ Scribed by N. Darin; A.-K. Kroksmark; A.-C. Åhlander; A.-R. Moslemi; A. Oldfors; M. Tulinius
- Book ID
- 113590213
- Publisher
- Elsevier Science
- Year
- 2007
- Tongue
- English
- Weight
- 598 KB
- Volume
- 11
- Category
- Article
- ISSN
- 1090-3798
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## Abstract ## Objective Defects in glycosylation of α‐dystroglycan are associated with several forms of muscular dystrophy, often characterized by congenital onset and severe structural brain involvement, collectively known as dystroglycanopathies. Six causative genes have been identified in thes
## Background Limb girdle muscular dystrophies (LGMD) are inclusive of 7 autosomal dominant and 14 autosomal recessive disorders featuring progressive muscle weakness and atrophy. Studies of cardiac function have not yet been well-defined in deficiencies of dysferlin (LGMD2B) and fukutin related pr