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dc.contributor.authorDenais, Cen_US
dc.contributor.authorDent, CLen_US
dc.contributor.authorSouthgate, Len_US
dc.contributor.authorHoyle, Jen_US
dc.contributor.authorDafou, Den_US
dc.contributor.authorTrembath, RCen_US
dc.contributor.authorMachado, RDen_US
dc.date.accessioned2016-03-21T12:07:41Z
dc.date.issued2011-02en_US
dc.identifier.issn1059-7794en_US
dc.identifier.urihttp://qmro.qmul.ac.uk/xmlui/handle/123456789/11534
dc.description.sponsorshipThe British Heart Foundation. Grant Number: RG/08/006/25302 (to R.C.T.); FS/07/036 (to R.D.M.); FS/06/051 (to C.D.).en_US
dc.format.extent231 - 239en_US
dc.relation.ispartofHUM MUTATen_US
dc.subjectDymeclinen_US
dc.subjectSkeletal dysplasiaen_US
dc.subjectsecretionen_US
dc.subjectchondrogenesisen_US
dc.subjectGolgien_US
dc.subjectSMITH-MCCORT-DYSPLASIAen_US
dc.subjectCELL-FREE SYSTEMen_US
dc.subjectMENTAL-RETARDATIONen_US
dc.subjectCYCLOPHILIN-Ben_US
dc.subjectGROWTH-PLATEen_US
dc.subjectMUTATIONSen_US
dc.subjectSTACKINGen_US
dc.subjectDISORDERSen_US
dc.subjectZEBRAFISHen_US
dc.subjectCISTERNAEen_US
dc.titleDymeclin, the Gene Underlying Dyggve-Melchior-Clausen Syndrome, Encodes a Protein Integral to Extracellular Matrix and Golgi Organization and is Associated with Protein Secretion Pathways Critical in Bone Developmenten_US
dc.typeArticle
dc.rights.holder© 2011 Wiley-Liss, Inc.
dc.identifier.doi10.1002/humu.21413en_US
pubs.issue2en_US
pubs.notesNot knownen_US
pubs.volume32en_US


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