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The Biochemical Journal|April 15, 1995
Two site-directed mutations abrogate enzyme activity but have different effects on the conformation and cellular content of the N-acetylgalactosamine 4-sulphatase proteinD A Brooks, D A Robertson, C Bindloss, et al.
Lancet (London, England)|February 4, 1984
Characterisation and use of an intragenic polymorphic marker for detection of carriers of haemophilia B (factor IX deficiency)F Giannelli, D S Anson, K H Choo, et al.
Neuromuscular Disorders : NMD|July 1, 1997
Canine fucosidosis: a model for retroviral gene transfer into haematopoietic stem cellsM L Ferrara, T Occhiodoro, M Fuller, et al.
Gene Therapy|May 1, 1997
In vitro correction of iduronate-2-sulfatase deficiency by adenovirus-mediated gene transferC Di Francesco, C Cracco, R Tomanin, et al.
Gene Therapy|February 16, 2007
Lentivirus-mediated gene transfer to the rat, ovine and human corneaD G A Parker, C Kaufmann, H M Brereton, et al.
The Journal of Clinical Investigation|April 15, 1996
Enzyme replacement therapy in a feline model of Maroteaux-Lamy syndromeA C Crawley, D A Brooks, V J Muller, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 5, 1996
Long-term in vitro correction of alpha-L-iduronidase deficiency (Hurler syndrome) in human bone marrowL J Fairbairn, L S Lashford, E Spooncer, et al.
Casopis Lekaru Ceskych|January 8, 1997
Towards gene therapy of Hurler syndromeL J Fairbairn, L S Lashford, E Spooncer, et al.
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