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https://hdl.handle.net/2440/17331
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Full metadata record
DC Field | Value | Language |
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dc.contributor.author | Whitfield, Phillip D. | en |
dc.contributor.author | Calvin, J. | en |
dc.contributor.author | Hogg, S. | en |
dc.contributor.author | O'Driscoll, E. | en |
dc.contributor.author | Halsall, D. | en |
dc.contributor.author | Burling, K. | en |
dc.contributor.author | Macguire, G. | en |
dc.contributor.author | Wright, N. | en |
dc.contributor.author | Cox, T. M. | en |
dc.contributor.author | Meikle, Peter John | en |
dc.contributor.author | Deegan, P. B. | en |
dc.date.issued | 2005 | en |
dc.identifier.citation | Journal of Inherited Metabolic Disease, 2005; 28:21-33 | en |
dc.identifier.issn | 0141-8955 | en |
dc.identifier.uri | http://hdl.handle.net/2440/17331 | - |
dc.language.iso | en | en |
dc.publisher | Kluwer Academic Publ | en |
dc.title | Monitoring enzyme replacement therapy in Fabry disease - Role of urine globotriaosylceramide | en |
dc.type | Journal article | en |
dc.contributor.school | School of Paediatrics and Reproductive Health : Paediatrics | en |
dc.identifier.doi | 10.1007/s10545-005-4415-x | en |
Appears in Collections: | Paediatrics publications |
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