| Literature DB >> 8364702 |
Abstract
Myotonic dystrophy is the commonest inherited muscle disease of adults. It causes significant clinical features in many organ systems and requires a broad-based approach for optimum management. Recent genetic advances promise to provide exciting new insights into the pathophysiology of the disease and may allow rational treatments to be developed.Entities:
Mesh:
Year: 1993 PMID: 8364702
Source DB: PubMed Journal: Br J Hosp Med ISSN: 0007-1064