Fluorophore-assisted electrophoresis of urinary carbohydrates for the identification of patients with oligosaccharidosis-and mucopolysaccharidosis-type lysosomal storage diseases

Author:

Starr Christopher M.,Klock John C.,Skop Elisa,Masada Irene,Giudici Tullio

Publisher

Springer Science and Business Media LLC

Reference43 articles.

1. Sweetman L. Genetic metabolic disorders. In: Soldin SJ, Rifia N and Hicks JMB, eds.Biochemical Basis of Pediatric Disease. Washington DC: AACC Press, 1992; 359–95.

2. Neufeld EF. Lysosomal storage diseases.Ann Rev Biochem 1991:60; 257–80.

3. Hommes FA, ed.Techniques in Diagnostic Human Biochemical Genetics. New York: Wiley-Liss, 1991; 69–219.

4. Watts RWE, Gibbs DA, eds.Lysosomal Storage Diseases: Biochemical and Clinical Aspects. London: Taylor & Francis, 1986; 1.

5. Wenger DA, Williams C. Screening for lysosomal disorders. In: Hommes FA, ed.Techniques in Diagnostic Human Biochemical Genetics. New York: Wiley-Liss, 1991; 587–617.

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