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Clinical Trials on Pyruvate Carboxylase Deficiency

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    • NCT01461304
      No longer available
      Compassionate Use of Triheptanoin (C7) for Inherited Disorders of Energy Metabolism
      Conditions: Very Long-chain acylCoA Dehydrogenase (VLCAD) Deficiency; Carnitine Palmitoyltransferase Deficiencies (CPT1, CPT2); Mitochondrial Trifunctional Protein Deficiency; Long-chain Hydroxyacyl-CoA Dehydrogenase Deficiency; Glycogen Storage Disorders; Pyruvate Carboxylase Deficiency Disease; ACYL-CoA DEHYDROGENASE FAMILY, MEMBER 9, DEFICIENCY of; Barth Syndrome
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