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Samples in periodicals archive:
Through a joint research effort with the Neurogenetics Branch of the NINDS, ASC will use the funding to pursue development of an oral drug treatment for spinal and bulbar muscular atrophy (SBMA) or Kennedy's Disease, a rare hereditary neurodegenerative disease, which currently has no approved drug available to patients.
A team of Japanese researchers has discovered clues as to how some neurodegenerative diseases occur, possibly paving the way for effective medical treatment of nervous disorders such as Huntington's disease and spinal and bulbar muscular atrophy.