Deficiency of propionyl-CoA carboxylase and methylcrotonyl-CoA carboxylase in a patient with methylcrotonylglycinuria

This publication has 17 references indexed in Scilit:

• Child with a defect in leucine metabolism associated with beta-hydroxyisovaleric aciduria and beta-methylcrotonylglycinuria.
  Archives of Disease in Childhood, 1973
• Some properties of propionyl CoA carboxylase partially purified from human liver
  Biochemical Medicine, 1973
• Evidence for the enzymic defect in β‐methylcrotonylglycinuria
  FEBS Letters, 1973
• Chemical synthesis of carnitine and coenzyme a esters of the β-substituted intermediates of hexadecanoic acid metabolism
  Biochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism, 1971
• BIOTIN-RESPONSIVE β-METHYLCROTONYLGLYCINURIA
  The Lancet, 1971
• $beta;-HYDROXYISOVALERIC ACIDURIA AND $beta;-METHYLCROTONYLGLYCINURIA: A NEW INBORN ERROR OF METABOLISM
  The Lancet, 1970
• An improved nutrient solution for diploid Chinese hamster and human cell lines
  Experimental Cell Research, 1963
• A simple efficient liquid scintillator for counting aqueous solutions in a liquid scintillation counter
  Analytical Biochemistry, 1960
• Amino Acid Metabolism in Mammalian Cell Cultures
  Science, 1959
• The Preparation of S-Succinyl Coenzyme A
  Journal of the American Chemical Society, 1953