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1909 wurde die klassische myotone Dystrophie (DM1) von Steinert erstmals beschrieben, 1994 entdeckte Ricker eine 2. Form (DM2). Als genetische Ursache der DM1 wurde 1992 ein abnorm expandiertes CTG(Cytosin-Thymin-Guanin)-Triplett-Repeat im 3’-UTR des Dystrophia-myotonica-Proteinkinase-Gens (DMPK-Gen) auf Chromosom 19 entdeckt, während 2001 die DM2 auf ein abnorm expandiertes Tetranukleotid-CCTG-Repeat...
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