Limb girdle muscular dystrophies: classification, clinical spectrum and emerging therapies
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Neurology (clinical),Neurology
Reference44 articles.
1. On the classification, natural history and treatment of the myopathies;Walton;Brain,1954
2. LGMD2I presenting with a characteristic Duchenne or Becker dystrophy phenotype;Schwartz;Neurology,2005
3. Mutations in the proteolytic enzyme calpain 3 cause limb-girdle muscular dystrophy type 2A;Richard;Cell,1995
4. Calpains and disease;Zatz;N Engl J Med,2005
5. Prevalence of genetic muscle disease in Northern England: in-depth analysis of a muscle clinic population;Norwood;Brain,2009
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