A variant form of citrullinemia.

[1]  N. Kennaway,et al.  Citrullinemia: Enzymatic Evidence for Genetic Heterogeneity , 1975, Pediatric Research.

[2]  M. Mihatsch,et al.  Variants of citrullinaemia. , 1973, Archives of disease in childhood.

[3]  K. Hirokawa,et al.  [An autopsy case of juvenile hepato-cerebral degeneration (non-Wilsonian Inose-type) with mental retardation, with special reference to ammonia and amino acids metabolism (author's transl)]. , 1973, Seishin shinkeigaku zasshi = Psychiatria et neurologia Japonica.

[4]  B. Brown,et al.  Metabolic and biochemical studies in fructose 1,6-diphosphatase deficiency. , 1973, The Journal of pediatrics.

[5]  J. Higgins,et al.  Citrullinemia: a new case, with implications concerning adaptation to defective urea synthesis. , 1972, Pediatric research.

[6]  L. Monnens,et al.  Citrullinaemia with Rapidly Fatal Neonatal Course , 1971, Archives of disease in childhood.

[7]  Y. Takekoshi,et al.  Hyperammonemia due to a mutant enzyme of ornithine transcarbamylase. , 1971, Pediatrics.

[8]  T. Tedesco,et al.  Argininosuccinate synthetase activity and citrulline metabolism in cells cultured from a citrullinemic subject. , 1967, Proceedings of the National Academy of Sciences of the United States of America.

[9]  S. Colowick,et al.  Methods in Enzymology , Vol , 1966 .

[10]  R. Schimke.  ENZYMES OF ARGININE METABOLISM IN MAMMALIAN CELL CULTURE. I. REPRESSION OF ARGININOSUCCINATE SYNTHETASE AND ARGININOSUCCINASE. , 1964, The Journal of biological chemistry.