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    4/13/2009 - New Therapeutic Strategy Could Target Toxic Protein In Most Patients With Huntington's Disease
    Posted in Medical News

    Howard Hughes Medical tenet researchers have designed tiny RNA molecules that shut off the gene that causes Huntington's disease without damaging that gene's healthy counterpart, which maintains the health and vitality of neurons. Laboratory studies suggest that a single small interfering RNA could reduce result of the damaging Huntingtin protein in nearly half of people with the disease.

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