Pharyngoesophageal motor function in patients with myotonic dystrophy
β Scribed by Dr. H. M. Swick; S. L. Werlin; W. J. Dodds; W. J. Hogan
- Publisher
- John Wiley and Sons
- Year
- 1981
- Tongue
- English
- Weight
- 379 KB
- Volume
- 10
- Category
- Article
- ISSN
- 0364-5134
No coin nor oath required. For personal study only.
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Length of (CTG)n triplet repeats in myotonic dystrophy protein kinase gene (DMPK) was estimated in tumors, normal tissues of the same organs, muscles, and leukocytes from three myotonic dystrophy (DM) patients and a non-DM patient. Using cDNA 25 as a probe, a Southern blot analysis of EcoRI- and Bgl
Myotonic dystrophy (DM) is an autosomal dominant disorder characterized by highly variable clinical features that include myotonia, progressive muscle weakness, smooth muscle involvement, hypersomnia, testicular atrophy, endocrine abnormalities, cardiac conduction blocks, and ~a t a r a c t . ~ The