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MDSG has provided a grant of £7,500 to help establish a Patient Registry for Myotonic Dystrophy in the UK, for which 'ethical approval' has now been achieved. Based in Newcastle, under the direction of Prof.Hanns Lochmuller, the registry will be an essential pre-requisite to future human trials of therapies for the condition. The Muscular Dystrophy Campaign has underwritten a similar sum. Watch out for news of the Registry’s progress to be published here during the coming months.
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