Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/87387
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dc.contributor.authorLiu, R.-
dc.contributor.authorvan der Lei, H.-
dc.contributor.authorWang, X.-
dc.contributor.authorWortham, N.-
dc.contributor.authorTang, H.-
dc.contributor.authorvan Berkel, C.-
dc.contributor.authorMufunde, T.-
dc.contributor.authorHuang, W.-
dc.contributor.authorvan der Knaap, M.-
dc.contributor.authorScheper, G.-
dc.contributor.authorProud, C.-
dc.date.issued2011-
dc.identifier.citationHuman Mutation, 2011; 32(9):1036-1045-
dc.identifier.issn1059-7794-
dc.identifier.issn1098-1004-
dc.identifier.urihttp://hdl.handle.net/2440/87387-
dc.description.abstractAbstract not available-
dc.description.statementofresponsibilityRui Liu, Hannemieke D.W. van der Lei, Xuemin Wang, Noel C. Wortham, Hua Tang, Carola G.M. van Berkel, Tsitsi Arikana Mufunde, Weida Huang, Marjo S. van der Knaap, Gert C. Scheper and Christopher G. Proud-
dc.language.isoen-
dc.publisherWiley-
dc.rights© 2011 Wiley-Liss, Inc.-
dc.source.urihttp://dx.doi.org/10.1002/humu.21535-
dc.subjectVWM; CACH; childhood ataxia with central nervous system hypomyelination; translation initiation factor-
dc.titleSeverity of vanishing white matter disease does not correlate with deficits in eIF2B activity or the integrity of eIF2B complexes-
dc.typeJournal article-
dc.identifier.doi10.1002/humu.21535-
pubs.publication-statusPublished-
dc.identifier.orcidProud, C. [0000-0003-0704-6442]-
Appears in Collections:Aurora harvest 7
Molecular and Biomedical Science publications

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