Arginase deficiency in a 12-year-old boy with mild impairment of intellectual function

Author:

Bernar Juan,Hanson Rebecca A.,Kern Rita,Phoenix Betsy,Shaw Kenneth N.F.,Cederbaum Stephen D.

Publisher

Elsevier BV

Subject

Pediatrics, Perinatology and Child Health

Reference12 articles.

1. Urea cycle disorders and other hereditary hyperammonemic syndromes;Walser,1983

2. A new French-Canadian family affected by hyperargininemia;Quereshi;J Inherited Metab Dis,1983

3. Hyperargininemia: effect of ornithine and lysine supplementation;Kang;J Pediatr,1983

4. Argininemia: report of a new case and mechanisms of orotic aciduria and hyperammonemia;Yoshino,1982

5. Diagnosis and treatment of argininemia. Characteristics of arginase in human erythrocytes and tissues;Endres;J Inherited Metab Dis,1984

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1. Clinical Features and Neurologic Progression of Hyperargininemia;Pediatric Neurology;2012-06

2. Argininemia;Atlas of Inherited Metabolic Diseases 3E;2011-12-30

3. Identification of two arginases generated by alternative splicing in the silkworm, Bombyx mori;Archives of Insect Biochemistry and Physiology;2010-12-06

4. Hyperargininemia due to liver arginase deficiency;Molecular Genetics and Metabolism;2005-03

5. Functional Consequences of the G235R Mutation in Liver Arginase Leading to Hyperargininemia;Archives of Biochemistry and Biophysics;2002-03

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