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Researchers suggest new approach to diagnose genetic muscle disease
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Researchers suggest new approach to diagnose genetic muscle disease
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Researchers at Washington University School of Medicine in St. Louis have developed an approach that could help doctors distinguish between the many subtypes of limb girdle muscular dystrophy, a rare, genetic muscle disease. With new therapies poised to enter the clinic, identifying the precise subtype is necessary to ensure access to the most appropriate treatment.
New approach has improved diagnosis of rare genetic muscle disease: Study
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New approach improves diagnosis of rare genetic muscle disease
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