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Myotonic dystrophy type 1 (DM1), the most common form of adult muscular dystrophy, is caused by anormal expansion of CTG trinucleotide repeats located in the 3′-untranslated region of the DMPK gene.(More)
Duchennes muscular dystrophy (DMD) presents a frequency of 1:3500 male live births. The gene is located in Xp21.2. It's has 2.5 Mb and 79 exons. Becker's muscular dystrophy (BMD) is a less frequent,(More)