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	41.	Towards gene therapy for hemophilia B. [electronic resource] by Anson, D S Hock, R A Austen, D Smith, K J Brownlee, G G Verma, I M Miller, A D Producer: 19870828 In: Molecular biology & medicine vol. 4 Availability: No items available. Save to lists Add to cart (remove)
	42.	Cloning and sequence analysis of caprine N-acetylglucosamine 6-sulfatase cDNA. [electronic resource] by Friderici, K Cavanagh, K T Leipprandt, J R Traviss, C E Anson, D S Hopwood, J J Jones, M Z Producer: 19950814 In: Biochimica et biophysica acta vol. 1271 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	43.	Two site-directed mutations abrogate enzyme activity but have different effects on the conformation and cellular content of the N-acetylgalactosamine 4-sulphatase protein. [electronic resource] by Brooks, D A Robertson, D A Bindloss, C Litjens, T Anson, D S Peters, C Morris, C P Hopwood, J J Producer: 19950526 In: The Biochemical journal vol. 307 ( Pt 2) Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	44.	Human alpha-L-iduronidase: cDNA isolation and expression. [electronic resource] by Scott, H S Anson, D S Orsborn, A M Nelson, P V Clements, P R Morris, C P Hopwood, J J Producer: 19911203 In: Proceedings of the National Academy of Sciences of the United States of America vol. 88 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	45.	Characterisation and use of an intragenic polymorphic marker for detection of carriers of haemophilia B (factor IX deficiency). [electronic resource] by Giannelli, F Anson, D S Choo, K H Rees, D J Winship, P R Ferrari, N Rizza, C R Brownlee, G G Producer: 19840504 In: Lancet (London, England) vol. 1 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	46.	Canine fucosidosis: a model for retroviral gene transfer into haematopoietic stem cells. [electronic resource] by Ferrara, M L Occhiodoro, T Fuller, M Hawthorne, W J Teutsch, S Tucker, V E Hopwood, J J Stewart, G J Anson, D S Producer: 19971009 In: Neuromuscular disorders : NMD vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	47.	In vitro correction of iduronate-2-sulfatase deficiency by adenovirus-mediated gene transfer. [electronic resource] by Di Francesco, C Cracco, C Tomanin, R Picci, L Ventura, L Zacchello, E Di Natale, P Anson, D S Hopwood, J J Graham, F L Scarpa, M Producer: 19970919 In: Gene therapy vol. 4 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	48.	Lentivirus-mediated gene transfer to the rat, ovine and human cornea. [electronic resource] by Parker, D G A Kaufmann, C Brereton, H M Anson, D S Francis-Staite, L Jessup, C F Marshall, K Tan, C Koldej, R Coster, D J Williams, K A Producer: 20070702 In: Gene therapy vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	49.	Enzyme replacement therapy in a feline model of Maroteaux-Lamy syndrome. [electronic resource] by Crawley, A C Brooks, D A Muller, V J Petersen, B A Isaac, E L Bielicki, J King, B M Boulter, C D Moore, A J Fazzalari, N L Anson, D S Byers, S Hopwood, J J Producer: 19960614 In: The Journal of clinical investigation vol. 97 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	50.	Towards gene therapy of Hurler syndrome. [electronic resource] by Fairbairn, L J Lashford, L S Spooncer, E McDermott, R H Lebens, G Arrand, J E Arrand, J R Bellantuono, I Holt, R Hatton, C E Cooper, A Besley, G T Wraith, J E Anson, D S Hopwood, J J Dexter, T M Producer: 19970514 In: Casopis lekaru ceskych vol. 136 Availability: No items available. Save to lists Add to cart (remove)
	51.	Long-term in vitro correction of alpha-L-iduronidase deficiency (Hurler syndrome) in human bone marrow. [electronic resource] by Fairbairn, L J Lashford, L S Spooncer, E McDermott, R H Lebens, G Arrand, J E Arrand, J R Bellantuono, I Holt, R Hatton, C E Cooper, A Besley, G T Wraith, J E Anson, D S Hopwood, J J Dexter, T M Producer: 19960905 In: Proceedings of the National Academy of Sciences of the United States of America vol. 93 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)