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    • Multiple Approaches to Novel GSD Ia Therapies 

      Landau, Dustin James (2016)
      Glycogen storage disease type Ia is an autosomal recessive disorder caused by a mutation in the glucose-6-phosphatase (G6Pase) catalytic subunit, encoded in humans by G6PC. G6Pase dephosphorylates glucose-6-phosphate (G6P) ...