Journal
Brain
Publication Date
12-1-2023
Volume
146
Issue
12
First Page
5198
Last Page
5208
Document Type
Open Access Publication
DOI
10.1093/brain/awad292
Rights and Permissions
Arthur Stefanski, Eduardo Pérez-Palma, Tobias Brünger, Ludovica Montanucci, Cornelius Gati, Chiara Klöckner, Katrine M Johannesen, Kimberly Goodspeed, Marie Macnee, Alexander T Deng, Ángel Aledo-Serrano, Artem Borovikov, Maina Kava, Arjan M Bouman, M J Hajianpour, Deb K Pal, Marc Engelen, Eveline E O Hagebeuk, Marwan Shinawi, Alexis R Heidlebaugh, Kathryn Oetjens, Trevor L Hoffman, Pasquale Striano, Amanda S Freed, Line Futtrup, Thomas Balslev, Anna Abulí, Leslie Danvoye, Damien Lederer, Tugce Balci, Maryam Nabavi Nouri, Elizabeth Butler, Sarah Drewes, Kalene van Engelen, Katherine B Howell, Jean Khoury, Patrick May, Marena Trinidad, Steven Froelich, Johannes R Lemke, Jacob Tiller, Amber N Freed, Jing-Qiong Kang, Arthur Wuster, Rikke S Møller, Dennis Lal, SLC6A1 variant pathogenicity, molecular function and phenotype: a genetic and clinical analysis, Brain, Volume 146, Issue 12, December 2023, Pages 5198–5208, https://doi.org/10.1093/brain/awad292. https://academic.oup.com/brain/article/146/12/5198/7255896?login=true. © The Author(s) 2023. Published by Oxford University Press on behalf of the Guarantors of Brain. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
Recommended Citation
Stefanski, Arthur; Shinawi, Marwan; and et al., "SLC6A1 variant pathogenicity, molecular function and phenotype: A genetic and clinical analysis." Brain. 146, 12. 5198 - 5208. (2023).
https://digitalcommons.wustl.edu/oa_4/2682
Department
ICTS (Institute of Clinical and Translational Sciences)
Additional Links
Supplemental material is available for this article at publisher site.
