Dymeclin, 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 Development
dc.contributor.author | Denais, C | en_US |
dc.contributor.author | Dent, CL | en_US |
dc.contributor.author | Southgate, L | en_US |
dc.contributor.author | Hoyle, J | en_US |
dc.contributor.author | Dafou, D | en_US |
dc.contributor.author | Trembath, RC | en_US |
dc.contributor.author | Machado, RD | en_US |
dc.date.accessioned | 2016-03-21T12:07:41Z | |
dc.date.issued | 2011-02 | en_US |
dc.identifier.issn | 1059-7794 | en_US |
dc.identifier.uri | http://qmro.qmul.ac.uk/xmlui/handle/123456789/11534 | |
dc.description.sponsorship | The 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.extent | 231 - 239 | en_US |
dc.relation.ispartof | HUM MUTAT | en_US |
dc.subject | Dymeclin | en_US |
dc.subject | Skeletal dysplasia | en_US |
dc.subject | secretion | en_US |
dc.subject | chondrogenesis | en_US |
dc.subject | Golgi | en_US |
dc.subject | SMITH-MCCORT-DYSPLASIA | en_US |
dc.subject | CELL-FREE SYSTEM | en_US |
dc.subject | MENTAL-RETARDATION | en_US |
dc.subject | CYCLOPHILIN-B | en_US |
dc.subject | GROWTH-PLATE | en_US |
dc.subject | MUTATIONS | en_US |
dc.subject | STACKING | en_US |
dc.subject | DISORDERS | en_US |
dc.subject | ZEBRAFISH | en_US |
dc.subject | CISTERNAE | en_US |
dc.title | Dymeclin, 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 Development | en_US |
dc.type | Article | |
dc.rights.holder | © 2011 Wiley-Liss, Inc. | |
dc.identifier.doi | 10.1002/humu.21413 | en_US |
pubs.issue | 2 | en_US |
pubs.notes | Not known | en_US |
pubs.volume | 32 | en_US |
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