1. Al Sawaf, S., Mayatepek, E., & Hoffmann, B. (2008). Neurological findings in Hunter disease: Pathology and possible therapeutic effects reviewed. Journal of Inherited Metabolic Disease, 31, 473–480.
2. Archer, I. M., Young, I. D., Rees, D. W., et al. (1983). Carrier detection in Hunter syndrome. American Journal of Medical Genetics, 16, 61–69.
3. Archer, I. M., Kingston, H. M., & Harper, P. S. (1984). Prenatal diagnosis of Hunter syndrome. Prenatal Diagnosis, 4, 195–200.
4. Beighton, P. (Ed.). (1993). Mckusick’s hereditable disorders of connective tissue (5th ed.). St. Louis: CV Mosby.
5. Bergstrom, S. K., Quinn, J. J., Greenstein, R., et al. (1994). Long-term follow-up of a patient transplanted for Hunter’s disease type IIB: A case report and literature review. Bone Marrow Transplantation, 14, 653–658.