N.K. and D.C. contributed equally to this work.
A novel X-linked disorder with developmental delay and autistic features
Article first published online: 28 DEC 2011
Copyright © 2011 American Neurological Association
Annals of Neurology
Volume 71, Issue 4, pages 498–508, April 2012
How to Cite
Kaya, N., Colak, D., Albakheet, A., Al-Owain, M., Abu-Dheim, N., Al-Younes, B., Al-Zahrani, J., Mukaddes, N. M., Dervent, A., Al-Dosari, N., Al-Odaib, A., Kayaalp, I. V., Al-Sayed, M., Al-Hassnan, Z., Nester, M. J., Al-Dosari, M., Al-Dhalaan, H., Chedrawi, A., Gunoz, H., Karakas, B., Sakati, N., Alkuraya, F. S., Gascon, G. G. and Ozand, P. T. (2012), A novel X-linked disorder with developmental delay and autistic features. Ann Neurol., 71: 498–508. doi: 10.1002/ana.22673
- Issue published online: 20 APR 2012
- Article first published online: 28 DEC 2011
- Accepted manuscript online: 25 NOV 2011 08:37AM EST
- Manuscript Accepted: 4 NOV 2011
- Manuscript Revised: 4 OCT 2011
- Manuscript Received: 27 AUG 2011
- King Faisal Specialist Hospital and Research Centre
Additional Supporting Information can be found in the online version of this article.
|ANA_22673_sm_SuppInfoFig1.pdf||614K||Supporting Information Figure 1: (A-C) The MRI and MRS brain images showing somewhat thinned corpus callosum and normal peaks of creatine, lactate, and N-acetylaspartate in left frontal lobe.|
|ANA_22673_sm_SuppInfoFig2.pdf||297K||Supporting Information Figure 2. X-Inactivation assays and aCGH results for grandmothers from family I and II and great grandmother from family I.|
|ANA_22673_sm_SuppInfoTab1.pdf||377K||Supplementary Table 1: List of 139 genes within the duplication at Xq12-q13.3|
|ANA_22673_sm_SuppInfoTab2.pdf||262K||Supplementary Table 2: Genes dysregulated in patients compared to controls|
|ANA_22673_sm_SuppInfoTab3.pdf||635K||Supplementary Table 3: Common genes between validation datasets and our global expression profiling analysis|
|ANA_22673_sm_SuppInfoTab4.pdf||321K||Supplementary Table 4: The overrepresented functional categories and disorders associated with common genes between independent ASD validation datasets and our differentially expressed genes.|
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