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Research Article

Maroteaux–Lamy Syndrome (Mucopolysaccharidosis VI) Presenting as Familial Myelopathy

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Pages 337-340 | Received 04 Oct 2010, Published online: 25 Feb 2011

REFERENCES

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  • Jin, W. D., Jackson, C. E., Desnick, R. J., & Schuchman, E. H. (1992). Mucopolysaccharidosis type VI: Identification of three mutations in the arylsulfatase B gene of patients with the severe and mild phenotypes provides molecular evidence for genetic heterogeneity. American Journal of Human Genetics, 50, 795–800.
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