Prenatal diagnosis for arginase deficiency: A case study-Reference-Cited by-同舟云学术

Prenatal diagnosis for arginase deficiency: A case study

Published:2003-09 Issue:6 Volume:26 Page:607-610
ISSN:0141-8955
Container-title:Journal of Inherited Metabolic Disease
language:en
Short-container-title:J Inherit Metab Dis

Author:

Hewson S.¹²,Clarke J. T. R.¹,Cederbaum S.³

Affiliation:

1. ; Division of Clinical and Metabolic Genetics; The Hospital for Sick Children, and the University of Toronto; Toronto Ontario Canada

2. ; Division of Clinical and Metabolic Genetics; The Hospital for Sick Children; 555 University Avenue Toronto ON M5G 1X8 Canada

3. ; Departments of Psychiatry, Pediatrics and Human Genetics and The Mental Retardation Research Center; University of California; Los Angeles California USA

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1023/A:1025964401618/fullpdf

Reference17 articles.

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2. Cloning of rat liver arginase cDNA and the elucidation of the regulation of arginase gene expression in H4 rat hepatoma cells;Dizikes;Somat Cell Mol Genet,1986

3. Molecular cloning of cDNA for non-hepatic mitochondrial arginase (arginase II) and comparison of its induction with nitric oxide synthase in a murine macrophage-like cell line;Gotoh;FEBS Lett,1996

4. Differential expression of the two human arginase genes in hyperargininaemia: enzymatic, pathologic, and molecular analysis;Grody;J Clin Invest,1989

5. Molecular genetic study of human arginase deficiency;Grody;Am J Hum Genet,1992

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