1. Neufeld, E.R and Muenzer, J. (1995) The mucopolysaccharidoses, in The Metabolic and Molecular Bases of Inherited Disease (eds C.R. Scriver, A.L. Beaudet, W.S. Sly and D. Valle). McGraw-Hill, New York, pp. 2465–2494.
2. Meikle, P.J., Hopwood, J.J., Clague, A.E., Carey, W.F. (1999) Prevalence of lysosomal storage disorders. JAMA 281, 249–254.
3. van de Kamp, J.J., Niermeijer, M.E, von Figura, K., Giesberts, M.A., (1981) Genetic heterogeneity and clinical variable in the Sanfilippo syndrome (types A, B, and C). Clin. Genet. 20, pp. 152–160.
4. Ullrich, K. and Kresse, H. (1996) Mucopolysaccharidoses, in Physican’s Guide to the laboratory diagnosis of metabolic diseases (eds N. Blau, M. Duran, M.E. Blaskovics). Chapman and Hall Medical, New York, pp. 303–317.
5. Whitley, C.B. (1993) The mucopolysaccharidoses, in McKusick’s Heritable Disorders of Connective Tissue (P. Beighton), 5th edition, St. Louis, CV Mosby, pp. 367–499.