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This Concept Map, created with IHMC CmapTools, has information related to: mark davis_a7 final, Deletion within the dystrophin gene (Xp21 locus) at exons 46-51 Characteristic of Duchenne's Muscular Dystrophy, Diagnostic studies of Genetic analysis, new open reading frame allowing for transcript stability, single base pair mutation of Xp21.1-2 causes premature stop codon, positive Babinski sign (down-going bilaterally) indicating Central Nervous System Problems, Induced Exon skipping which alters mRNA splicing, 25,000 IU/L Characteristic of Duchenne's Muscular Dystrophy, calcium signaling activates calcium sensitive enzymes, protein with residual dystrophin function mimicking Becker's Muscular Dystrophy Phenotype, Clusters of necrotic and regenerating muscle fibers, severe proliferation of fibrous, fatty connective tissue with mononuclear inflammatory infiltrates Characteristic of Duchenne's Muscular Dystrophy, Genetic analysis showed Deletion within the dystrophin gene (Xp21 locus) at exons 46-51, Diagnostic studies of Western Blot, Diagnostic studies including EKG, cardiomyopathy Characteristic of Duchenne's Muscular Dystrophy, mRNA splicing to exclude mutated exon, calcium sensitive enzymes such as proteases, premature stop codon and an altered genetic sequence, calcium sensitive enzymes such as Endonuclease, calcium sensitive enzymes causes generalized motor and muscle atrophy, Diagnostic studies for creatine kinase