Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/17372
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dc.contributor.authorCrane, Denis I.en
dc.contributor.authorMaxwell, Megan A.en
dc.contributor.authorPaton, Barbara Clelanden
dc.date.issued2005en
dc.identifier.citationHuman Mutation. 26:167-175en
dc.identifier.issn1059-7794en
dc.identifier.urihttp://hdl.handle.net/2440/17372-
dc.language.isoenen
dc.publisherWiley-Lissen
dc.titlePEX1 mutations in the Zellweger spectrum of the peroxisome biogenesis disordersen
dc.typeJournal articleen
dc.contributor.schoolSchool of Paediatrics and Reproductive Health : Paediatricsen
dc.identifier.doi10.1002/humu.20211en
Appears in Collections:Paediatrics publications

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