These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
3. Identification of mutations (D128G, H141L) in the liver arginase gene of patients with hyperargininemia. Vockley JG; Tabor DE; Kern RM; Goodman BK; Wissmann PB; Kang DS; Grody WW; Cederbaum SD Hum Mutat; 1994; 4(2):150-4. PubMed ID: 7981719 [No Abstract] [Full Text] [Related]
4. Use of enzyme-loaded erythrocytes in in-vitro correction of arginase-deficient erythrocytes in familial hyperargininemia. Adriaenssens K; Karcher D; Lowenthal A; Terheggen HG Clin Chem; 1976 Mar; 22(3):323-6. PubMed ID: 1253407 [TBL] [Abstract][Full Text] [Related]
5. [Hyperargininemia with arginase deficiency. A new familial metabolic disease. II. Biochemical studies]. Terheggen HG; Schwenk A; Lowenthal A; van Sande M; Colombo JP Z Kinderheilkd; 1970; 107(4):313-23. PubMed ID: 5438972 [No Abstract] [Full Text] [Related]
6. A new case of arginase deficiency in a Spanish male. Jordá A; Rubio V; Portolés M; Vilas J; García-Piño J J Inherit Metab Dis; 1986; 9(4):393-7. PubMed ID: 3104676 [TBL] [Abstract][Full Text] [Related]
7. Human hyperargininemia: a mutation not expressed in skin fibroblasts? Van Elsen AF; Leroy JG Am J Hum Genet; 1977 Jul; 29(4):350-5. PubMed ID: 879168 [TBL] [Abstract][Full Text] [Related]