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Furthermore, duchenne muscular dystrophy (DMD) is a progressive, genetic (X-linked recessive) neuromuscular disorder caused by mutations to the DMD gene, resulting in the dysfunction or absence of the dystrophin protein. This aspect of Duchenne Muscular Dystrophy Treatment A Support Guide plays a vital role in practical applications.
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Moreover, duchenne muscular dystrophy is a rare, genetic condition that is characterized by progressive muscle damage and weakness. Sometimes shortened to DMD or Duchenne, this rare disease is caused by a genetic mutation that prevents the body from producing a protein called dystrophin. This aspect of Duchenne Muscular Dystrophy Treatment A Support Guide plays a vital role in practical applications.
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Final Thoughts on Duchenne Muscular Dystrophy Treatment A Support Guide
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