Development of novel therapeutics for the treatment of the genetic disorder Spinal Muscular Atrophy

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Development of novel therapeutics for the treatment of the genetic disorder Spinal Muscular Atrophy

Development of novel therapeutics for the treatment of the genetic disorder Spinal Muscular Atrophy

Dr. Otis Vacratsis

University of Windsor

FUNDER: CIHR

GRANT DURATION: 2018-2020

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