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.
6. Molecular basis of hyperargininemia: structure-function consequences of mutations in human liver arginase. Ash DE; Scolnick LR; Kanyo ZF; Vockley JG; Cederbaum SD; Christianson DW Mol Genet Metab; 1998 Aug; 64(4):243-9. PubMed ID: 9758714 [TBL] [Abstract][Full Text] [Related]
7. Familial hyperargininemia. Terheggen HG; Lavinha F; Colombo JP; Van Sande M; Lowenthal A J Genet Hum; 1972 Mar; 20(1):69-84. PubMed ID: 4643877 [No Abstract] [Full Text] [Related]
8. [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]
9. [Hyperargininemia wityh arginase deficiency. A new familial metabolic disease. I. Clinical studies]. Terheggen HG; Schwenk A; Lowenthal A; van Sande M; Colombo JP Z Kinderheilkd; 1970; 107(4):298-312. PubMed ID: 5438971 [No Abstract] [Full Text] [Related]
10. Identification of a novel R21X mutation in the liver-type arginase gene (ARG1) in four Portuguese patients with argininemia. Cardoso ML; Martins E; Vasconcelos R; Vilarinho L; Rocha J Hum Mutat; 1999 Oct; 14(4):355-6. PubMed ID: 10502833 [TBL] [Abstract][Full Text] [Related]
11. 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]
12. Molecular basis of phenotypic variation in patients with argininemia. Uchino T; Snyderman SE; Lambert M; Qureshi IA; Shapira SK; Sansaricq C; Smit LM; Jakobs C; Matsuda I Hum Genet; 1995 Sep; 96(3):255-60. PubMed ID: 7649538 [TBL] [Abstract][Full Text] [Related]