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Top suggestions for Duchenne Muscular Dystrophy Genetics
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Duchenne Muscular Dystrophy
Duchenne is caused by a change or mutation in the gene that encodes instructions for creating dystrophin, an essential protein for muscle strength. Learn more about the disease and our research programs.
Sep 7, 2021
Duchenne Muscular Dystrophy Symptoms
The Critical Role of Dystrophin in the Pathophysiology of Duchenne Muscular Dystrophy | NeurologyLive - Clinical Neurology News and Neurology Expert Insights
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💡 What does “severe phenotype” mean in Duchenne muscular dystrophy (DMD)? When doctors talk about a phenotype, they’re referring to the way a condition shows up in someone’s body, the physical traits and symptoms that result from their genetics. In Duchenne, a severe phenotype usually means the condition progresses more quickly, often with earlier loss of abilities like walking, climbing stairs, or raising arms. This can also bring earlier complications with breathing, heart health, and other a
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