Concepedia

Hurler syndrome: A patient with abnormally high levels of α-l-iduronidase protein

Doug A. Brooks, G. S. Harper, G J Gibson, LJ Ashton, Jacqueline Taylor, P.A.G. McCouri, Craig Freeman, Peter R. Clements, Jürgen Hoffmann, John J. Hopwood

Biochemical Medicine and Metabolic Biology · 1992 · 19 citations · 24 references

DOI

Concepts

References

24

The Metabolic Basis of Inherited Disease

Annals of Internal Medicine · 1990 · 4K citations

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The Metabolic Basis of Inherited Disease.

Annals of Internal Medicine · 1983 · 2.7K citations

, , +13

Studies on glucosaminidase. 4. The fluorimetric assay of <i>N</i>-acetyl-β-glucosaminidase

David H. Leaback, P. G. Walker · Biochemical Journal · 1961 · 453 citations · Full text

, , +6

Partial Enzyme Deficiencies: Residual Activities and the Development of Neurological Disorders

Ernst Conzelmann, Konrad Sandhoff · Developmental Neuroscience · 2007 · 275 citations

, , +12

Human alpha-L-iduronidase: cDNA isolation and expression.

Hamish S. Scott, D S Anson, Annette Orsborn et al. · Proceedings of the National Academy of Sciences · 1991 · 152 citations

, , +14