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dc.contributor.authorKalscheuer, V.-
dc.contributor.authorIqbal, Z.-
dc.contributor.authorHu, H.-
dc.contributor.authorHaas, S.-
dc.contributor.authorShaw, M.-
dc.contributor.authorLebrun, N.-
dc.contributor.authorSeemanova, E.-
dc.contributor.authorVoesenek, K.-
dc.contributor.authorHobson, L.-
dc.contributor.authorRopers, H.H.-
dc.contributor.authorTownshend, S.-
dc.contributor.authorRaynaud, M.-
dc.contributor.authorvan Bokhoven, H.-
dc.contributor.authorRiazuddin, S.-
dc.contributor.authorChelly, J.-
dc.contributor.authorGecz, J.-
dc.identifier.citationJournal of Medical Genetics, 2013; 49(5):332--
dc.descriptionLetter to the Editor-
dc.description.statementofresponsibilityVera M. Kalscheuer, Z. Iqbal, H. Hu, S.A. Haas, M. Shaw, N. Lebrun, E. Seemanova, K. Voesenek, L. Hobson, H.H. Ropers, S. Townshend, M. Raynaud, H. van Bokhoven, S. Riazuddin, J. Chelly, J. Gecz-
dc.publisherBMJ Publishing Group-
dc.rightsCopyright status unknown-
dc.titleRAB40AL loss-of-function mutation does not cause X-linked intellectual disability-
dc.typeJournal article-
dc.identifier.orcidShaw, M. [0000-0002-5060-190X]-
dc.identifier.orcidGecz, J. [0000-0002-7884-6861]-
Appears in Collections:Aurora harvest
Paediatrics publications

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