Journal
HGG Advances
Publication Date
10-13-2022
Volume
3
Issue
4
First Page
100131
Document Type
Open Access Publication
DOI
10.1016/j.xhgg.2022.100131
Rights and Permissions
Mukherjee S, Cassini TA, Hu N, Yang T, Li B, Shen W, Moth CW, Rinker DC, Sheehan JH, Cogan JD; Undiagnosed Diseases Network; Newman JH, Hamid R, Macdonald RL, Roden DM, Meiler J, Kuenze G, Phillips JA, Capra JA. Personalized structural biology reveals the molecular mechanisms underlying heterogeneous epileptic phenotypes caused by de novo KCNC2 variants. HGG Adv. 2022 Jul 19;3(4):100131. doi: 10.1016/j.xhgg.2022.100131. Copyright 2022 The Author(s). This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
Recommended Citation
Mukherjee, Souhrid; Sheehan, Jonathan H; and et al., "Personalized structural biology reveals the molecular mechanisms underlying heterogeneous epileptic phenotypes caused by de novo KCNC2 variants." HGG Advances. 3, 4. 100131 (2022).
https://digitalcommons.wustl.edu/oa_4/3794
Additional Links
Supplemental material is available for this article at publisher site.
