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Investigating the potential role of CDK13 in the transcription and stability of mutant DMPK mRNA in myotonic dystrophy type 1
Myotonic Dystrophy (DM) is a complex multisystemic genetic disorder characterised by muscular dystrophy, myotonia and cardiorespiratory abnormalities. DM is classified as a repeat expansion disorder. DM type 1 is caused by a trinucleotide repeat expansion of CTG in the 3’untranslated region of the d
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