Transgenic overexpression of human DMPK accumulates into hypertrophic cardiomyopathy, myotonic myopathy and hypotension traits of myotonic dystrophy.

Source:http://linkedlifedata.com/resource/pubmed/id/15317754

Hum. Mol. Genet. 2004 Oct 15 13 20 2505-18

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PMID
15317754