• 13 June 1993
    • journal article
    • review article
    • Vol. 50  (1) , 22-30
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.

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