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124,316 Duchenne muscular dystrophy Duchenne muscular dystrophy (named after Guillaume-Benjamin-Amand Duchenne de Boulogne who provided early and comprehensive description of clinical presentation and histopathology of this disorder 317 ) is an X-linked recessive neuromuscular disorder caused by mutations in the DMD gene that encodes the protein dystrophin

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Acrolein contributes to TRPA1 up-regulation in peripheral and central sensory hypersensitivity following spinal cord injury

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Results can be seen in as little as 24-48 hours, depending on the severity of the injury