Six Serum miRNAs Fail to Validate as Myotonic Dystrophy Type 1 Biomarkers

Volume: 11, Issue: 2, Pages: e0150501 - e0150501
Published: Feb 26, 2016
Abstract
Myotonic dystrophy type 1 (DM1) is an autosomal dominant genetic disease caused by expansion of a CTG microsatellite in the 3' untranslated region of the DMPK gene. Despite characteristic muscular, cardiac, and neuropsychological symptoms, CTG trinucleotide repeats are unstable both in the somatic and germinal lines, making the age of onset, clinical presentation, and disease severity very variable. A molecular biomarker to stratify patients and...
Paper Details
Title
Six Serum miRNAs Fail to Validate as Myotonic Dystrophy Type 1 Biomarkers
Published Date
Feb 26, 2016
Journal
Volume
11
Issue
2
Pages
e0150501 - e0150501
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