Journal
Orphanet Journal of Rare Diseases
Publication Date
12-3-2019
Volume
14
Issue
1
First Page
279
Document Type
Open Access Publication
DOI
10.1186/s13023-019-1260-9
Rights and Permissions
Samara A, Rahn R, Neyman O, Park KY, Samara A, Marshall B, Dougherty J, Hershey T. Developmental hypomyelination in Wolfram syndrome: new insights from neuroimaging and gene expression analyses. Orphanet J Rare Dis. 2019 Dec 3;14(1):279. doi: 10.1186/s13023-019-1260-9. © The Author(s). 2019 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
Recommended Citation
Samara, Amjad; Rahn, Rachel; Neyman, Olga; Park, Ki Yun; Samara, Ahmad; Marshall, Bess; Dougherty, Joseph; and Hershey, Tamara, "Developmental hypomyelination in Wolfram syndrome: New insights from neuroimaging and gene expression analyses." Orphanet Journal of Rare Diseases. 14, 1. 279 (2019).
https://digitalcommons.wustl.edu/open_access_pubs/9109
Additional file 1. A list of the most highly correlated genes with WFS1 in BrainCloud database, available in CSEA dataset.
13023_2019_1260_MOESM2_ESM.jpg (4506 kB)
Additional file 2. Cell-type specific expression of WFS1 related genes in the CSEA dataset and derived from the BrainSpan database across several age groups.
13023_2019_1260_MOESM3_ESM.xlsx (45 kB)
Additional file 3. A list of biological processes from Gene ontology analysis of 4 month-4 years WFS1-related gene set using BiNGO, a biological network gene ontology tool.
