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Follow-up of three patients with a large in-frame deletion of exons 45–55 in the Duchenne muscular dystrophy (DMD) gene

Mendelian DisorderGenetic DisorderDuchenne Muscular DystrophyGeneticsMedicinePathologyLarge In-frame DeletionDegenerative DiseaseDisease Gene IdentificationNeuromuscular PathologyExons 45–55