The Newsroom    Published Tuesday, Jan. 21, 2014, 4:26 PM
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UT Medical Branch part of research team uncovering most detailed picture yet of muscular dystrophy defect, new targeted drug candidates

BioNews Texas, January 17, 2014

Researchers from UTMB, The Scripps Research Institute and Northwestern University have revealed an atomic-level view of a genetic defect that causes a form of muscular dystrophy known as myotonic dystrophy type 2. This information is being used to design drug candidates to counteract those defects.

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