Work Cited
1.Pan, D., Jonsson, J., Braun, S., Mclovr, R. & Whitley, C. "Supercharged Cells" for delivery of recombinant human iduronate-2-sulfatase. Mol Genet Metab 70, 170-178 (2015).
2.Wakabayashi, T. et al. Hematopoietic Stem Cell Gene Therapy Corrects Neuropathic Phenotype in Murine Model of Mucopolysaccharidosis Type II. Human Gene Therapy 26, 357-366 (2015).
1.Anekar, J., Narayanan, D., A.C., R., N.C., S. & Nappalli, D. A Rare Case of Mucopolysaccharidosis: Hunter Syndrome. JCDR 9, ZD23-ZD26 (2015). Available from: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4437174/
3.Burton, B. & Giugliani, R. Diagnosing Hunter syndrome in pediatric practice: practical considerations and common pitfalls. European Journal of Pediatrics 171, 631-639 (2012).
1.Pan, D., Jonsson, J., Braun, S., Mclovr, R. & Whitley, C. "Supercharged Cells" for delivery of recombinant human iduronate-2-sulfatase. Mol Genet Metab 70, 170-178 (2015).
2.Wakabayashi, T. et al. Hematopoietic Stem Cell Gene Therapy Corrects Neuropathic Phenotype in Murine Model of Mucopolysaccharidosis Type II. Human Gene Therapy 26, 357-366 (2015).
1.Anekar, J., Narayanan, D., A.C., R., N.C., S. & Nappalli, D. A Rare Case of Mucopolysaccharidosis: Hunter Syndrome. JCDR 9, ZD23-ZD26 (2015). Available from: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4437174/
3.Burton, B. & Giugliani, R. Diagnosing Hunter syndrome in pediatric practice: practical considerations and common pitfalls. European Journal of Pediatrics 171, 631-639 (2012).