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Monday, March 16, 2015

Targets identified for developing therapies for IBMPFD

IBMPFD is a rare and deadly genetic disorder that has devastated entire families, robbing many of their members of their ability to talk, walk and think clearly. A new study, which was published online today by the Proceedings of the National Academy of Sciences , offers new hope for these families because it has identified potential targets for developing therapies to treat this disorder, officially known as "Inclusion Body Myopathy with Paget's disease of bone and Frontotemporal Dementia."

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