gastrointestinal

A small-molecule compound counteracts some of the effects of abnormal genetic instructions in MMD1

posted on November 3, 2009 - 10:00pm
  A compound that has the potential to be refined and modified into a treatment for type 1 myotonic dystrophy (MMD1, or DM1) has been identified by researchers at the University of Oregon in Eugene, and the University of Rochester (N.Y.) School of Medicine and Dentistry.

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