The heart in muscular dystrophies
✍ Scribed by Finsterer, J. ;Stöllberger, Claudia
- Book ID
- 106064618
- Publisher
- Springer
- Year
- 2005
- Tongue
- German
- Weight
- 105 KB
- Volume
- 94
- Category
- Article
- ISSN
- 0300-5860
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📜 SIMILAR VOLUMES
## Abstract The purpose of this investigation was to compare the respiratory function of patients with different clinical types of muscular dystrophy (MD). A total of 190 patients representing facioscapulohumeral MD (__n__ = 20), limb‐girdle MD (__n__ = 50), Becker MD (__n__ = 20), Duchenne MD (__n
Mutations in the sarcoglycan genes cause autosomalrecessive muscular dystrophies. Because sarcoglycan genes and their protein products are highly expressed both in skeletal and cardiac muscle, patients with these mutations might be expected to be at risk to develop dilated cardiomyopathy. We therefo