Posted in Web Amino Acid Metabolism Disorders: MedlinePlus January 17, 2021 Understanding Hyperoxaluria (Oxalosis and Hyperoxaluria Foundation) Genetics 3-hydroxy-3-methylglutaryl-CoA lyase deficiency: MedlinePlus Genetics (National Library of Medicine) https://medlineplus.gov/aminoacidmetabolismdisorders.html